Compressed open flow assay and use

ABSTRACT

The present invention relates to the methods, devices, and systems that make bio/chemical sensing (including, not limited to, immunoassay, nucleic assay, electrolyte analysis, etc.) faster, more sensitive, less steps, easy to perform, smaller amount of samples required, less or reduced (or no) needs for professional assistance, and/or lower cost, than many current sensing methods and devices. The present invention also allow a test performed by a smartphone.

CROSS-REFERENCING

This application claims the benefit of U.S. Provisional Patent Application 62/456,065, filed on Feb. 7, 2017, U.S. Provisional Patent Application 62/456,504, filed on Feb. 8, 2017, U.S. Provisional Patent Application 62/459,972, filed on Feb. 16, 2017, and U.S. Provisional Patent Application 62/460,062, filed on Feb. 16, 2017, each of which applications are incorporated herein in their entireties for all purposes.

INCORPORATION BY REFERENCE OF SEQUENCE LISTING PROVIDED AS A TEXT FILE

A Sequence Listing is provided herewith as a text file, “ESX18 seq list_ST25.txt” created on November 19 and having a size of 2 KB. The contents of the text file are incorporated by reference herein in their entirety.

FIELD

The present invention is related to the field of bio/chemical sampling, sensing, assays and applications.

BACKGROUND

In biological and chemical assays (e.g. diagnostic testing), often it needs to measure the volume, change the shape, and/or detect analytes of a sample or a part of the sample, quickly and simply, in particularly high sample uniformity, which often leads to high assay accuracy. The current invention provides devices and methods for achieving these goals.

SUMMARY OF INVENTION

The following brief summary is not intended to include all features and aspects of the present invention. The present invention relates to the methods, devices, and systems that make bio/chemical sensing (including, not limited to, immunoassay, nucleic assay, electrolyte analysis, etc.) faster, more sensitive, less steps, easy to perform, smaller amount of samples required, less or reduced (or no) needs for professional assistance, and/or lower cost, than many current sensing methods and devices.

BRIEF DESCRIPTION OF THE DRAWINGS

The skilled artisan will understand that the drawings, described below, are for illustration purposes only. The drawings are not intended to limit the scope of the present teachings in any way. The drawings may not be in scale. In the figures that present experimental data points, the lines that connect the data points are for guiding a viewing of the data only and have no other means.

FIG. 1 is an illustration of a CROF (Compressed Regulated Open Flow) embodiment. Panel (a) illustrates a first plate and a second plate wherein the first plate has spacers. Panel (b) illustrates depositing a sample on the first plate (shown), or the second plate (not shown), or both (not shown) at an open configuration. Panel (c) illustrates (i) using the two plates to spread the sample (the sample flow between the plates) and reduce the sample thickness, and (ii) using the spacers and the plate to regulate the sample thickness at the closed configuration. The inner surface of each plate may have one or a plurality of binding sites and or storage sites (not shown).

FIG. 2 illustrates plates with a binding site or a storage site. Panel (a) illustrates a plate having a binding site. Panel (b) illustrates a plate having a reagent storage site. Panel (c) illustrates a first plate having a binding site and a second plate having a reagent storage site. Panel (d) illustrates a plate having multiple sites (binding sites and/or storage site).

FIG. 3 is a flow-chart and schematic of a method for reducing assay incubation time by reducing sample thickness. Panel (a) illustrates a first plate that has at least one binding site on a substrate surface. Panel (b) illustrates a second plate (which may have a different size from the first plate). Panel (c) illustrates depositing a sample (containing target binding entity) on the substrate surface (shown) or the cover plate (not shown), or both (not shown). Panel (d) illustrates moving the first and second plates so that they are facing each other, and reducing the sample thickness by reducing the spacing of the inner space between the plates. The reduced thickness sample is incubated. The reduced sample thickness speeds up the incubation time. Some embodiment of the method uses spacers to regulate the spacing, which (spacers) are not shown in the illustration.

FIG. 4 shows reducing binding or mixing time by reducing the sample thickness using two pates, spacers, and compression (shown in cross-section). Panel (a) illustrates reducing the time for binding entities in a sample to a binding site on a solid surface (X−(Volume to Surface)). Panel (b) illustrates reducing the time for binding entities (e.g. reagent) stored on a surface of plate to a binding site on a surface of another surface (X−(Surface to Surface)). Panel (c) illustrates reducing the time for adding reagents stored on a surface of a plate into a sample that is sandwiched between the plate and other plate (X−(Surface to Volume)).

FIG. 5 shows how to avoid or reduce local bending in a flexible plate. Panel (a) illustrates if the inter-spacer distance is too large for a flexible plate (the second plate, e.g. a plastic film) under a given set of sample and compress conditions, the plate has, at the closed configuration, a local sag (i.e. bending inward) between the two neighboring pacers, assuming the first plate is rigid. The sample between the plates is not drawn. Panel (b) illustrates local bending (sag) in a flexible plate in panel (a) is reduced or virtually avoided by using a proper inter-spacer distance and a proper compression force. The sample between the plates is not drawn.

FIG. 6 illustrates reducing effect of large dust on the plate spacing (sample thickness) regulation. Panel (a) illustrates When using two rigid plates, a dust with a thickness larger than a spacer height can destroy an intended plate spacing regulation by the spacers (hence destroy the intended sample thickness regulation). The sample between the plates is not drawn. Panel (b) illustrates using a proper flexible plate and a proper inter-spacer distance, the effect of a dust is isolated to a small area around dust, while in other areas, the plate spacing (hence the sample thickness) is regulated by the spacers not the dust. This illustration has the first plate is rigid, the second plate is flexible, and the spacers are initially fixed on the first plate. Panel (c) illustrates an illustration of using a proper flexible plate and a proper inter-spacer distance, the effect of a dust is isolated to a small area around dust, while in other areas, the plate spacing (hence the sample thickness) is regulated by the spacers not the dust. This illustration has the first plate is rigid, the second plate is flexible, and the spacers are initially fixed on the second plate.

FIG. 7 illustrates reducing effects of surface flatness variation of plate by using proper spacer arrangement and flexible plate(s). Panel (a) shows that surface flatness variation can be significantly large compared with a desired sample thickness, causing errors in determining a sample thickness. In this illustration, only one plate has a large flatness variation (in reality, both plates may have large flatness variation). The sample between the plates is not drawn. Panel (b) illustrates a surface flatness variation distance of a plate, □□, is the distance from a local maximum to a neighboring local minimum of a surface height. Panel (c) illustrates how a small surface flatness variation can be achieved by making one or both plate flexible and using a proper inter-spacer distance and proper compressing force to correct, at the closed configuration, the original surface flatness variation of the plate when they are at open configuration. The sample between the plates is not drawn. Panel (d) illustrates making the sample thickness variation less than the initial surface flatness variation of the plate by using a flexible second plate and a proper inter spacer distance. The flexible plate follows the contour of the rigid plate. The sample between the plates is not drawn.

FIG. 8 Spacers on a plate. Top view of photograph of (a) 46 um×46 um pillar spacer size and 54 um inter pillar distance, and (b) 10 um×70 um pillar spacer size and 10 um pillar distance; and prospect view SEM of (c) 30 um×40 um pillar spacer size of 2 um spacer height, and (d) 30 um×40 um pillar spacer size of 30 um spacer height.

FIG. 9. An illustration of certain aspects of an exemplary device and methods of collecting exhaled breath condensate (EBC) using a SiEBCA (Single-drop EBC Collector/Analyzer).

FIG. 10. An illustration of a SiEBCA with both “open spacer” and “enclosed spacer”, where the open spacer is a post (pillar) while the enclosed spacer is a ring spacer (d) and a four-chamber grid spacer (e).

FIG. 11. The surface wetting properties for an untreated and a treated (for better wetting than untreated surface) surface of a collection plate.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

The following detailed description illustrates some embodiments of the invention by way of example and not by way of limitation. The section headings and any subtitles used herein are for organizational purposes only and are not to be construed as limiting the subject matter described in any way. The contents under a section heading and/or subtitle are not limited to the section heading and/or subtitle, but apply to the entire description of the present invention.

The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present claims are not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided can be different from the actual publication dates which can need to be independently confirmed.

Compressed Regulated Open Flow” (CROF)

In assaying, a manipulation of a sample or a reagent can lead to improvements in the assaying. The manipulation includes, but not limited to, manipulating the geometric shape and location of a sample and/or a reagent, a mixing or a binding of a sample and a reagent, and a contact area of a sample of reagent to a plate.

Many embodiments of the present invention manipulate the geometric size, location, contact areas, and mixing of a sample and/or a reagent using a method, termed “compressed regulated open flow (CROF)”, and a device that performs CROF.

The term “compressed open flow (COF)” refers to a method that changes the shape of a flowable sample deposited on a plate by (i) placing other plate on top of at least a part of the sample and (ii) then compressing the sample between two plates by pushing the two plates towards each other; wherein the compression reduces a thickness of at least a part of the sample and makes the sample flow into open spaces between the plates.

The term “compressed regulated open flow” or “CROF” (or “self-calibrated compressed open flow” or “SCOF” or “SCCOF”) refers to a particular type of COF, wherein the final thickness of a part or entire sample after the compression is “regulated” by spacers, wherein the spacers, that are placed between the two plates.

The term “the final thickness of a part or entire sample is regulated by spacers” in a CROF means that during a CROF, once a specific sample thickness is reached, the relative movement of the two plates and hence the change of sample thickness stop, wherein the specific thickness is determined by the spacer.

One embodiment of the method of CROF, as illustrated in FIG. 1, comprises:

(a) obtaining a sample, that is flowable;

(b) obtaining a first plate and a second plate that are movable relative to each other into different configurations, wherein each plate has a sample contact surface that is substantially planar, wherein one or both of the plates comprise spacers and the spacers have a predetermined height, and the spacers are on a respective sample contacting surface;

(c) depositing, when the plates are configured in an open configuration, the sample on one or both of the plates; wherein the open configuration is a configuration in which the two plates are either partially or completely separated apart and the spacing between the plates is not regulated by the spacers; and

(d) after (c), spreading the sample by bringing the plates into a closed configuration, wherein, in the closed configuration: the plates are facing each other, the spacers and a relevant volume of the sample are between the plates, the thickness of the relevant volume of the sample is regulated by the plates and the spacers, wherein the relevant volume is at least a portion of an entire volume of the sample, and wherein during the sample spreading, the sample flows laterally between the two plates.

The term “plate” refers to, unless being specified otherwise, the plate used in a CROF process, which a solid that has a surface that can be used, together with another plate, to compress a sample placed between the two plate to reduce a thickness of the sample.

The term “the plates” or “the pair of the plates” refers to the two plates in a CROF process.

The term “first plate” or “second plate” refers to the plate use in a CROF process.

The term “the plates are facing each other” refers to the cases where a pair of plates are at least partially facing each other.

The term “spacers” or “stoppers” refers to, unless stated otherwise, the mechanical objects that set, when being placed between two plates, a limit on the minimum spacing between the two plates that can be reached when compressing the two plates together. Namely, in the compressing, the spacers will stop the relative movement of the two plates to prevent the plate spacing becoming less than a preset (i.e. predetermined) value. There are two types of the spacers: “open-spacers” and “enclosed-spacers”.

The term “open-spacer” means the spacer have a shape that allows a liquid to flow around the entire perimeter of the spacer and flow pass the spacer. For example, a pillar is an open spacer.

The term of “enclosed spacer” means the spacer of having a shape that a liquid cannot flow abound the entire perimeter of the spacer and cannot flow pass the spacer. For example, a ring shape spacer is an enclosed spacer for a liquid inside the ring, where the liquid inside the ring spacer remains inside the ring and cannot go to outside (outside perimeter).

The term “a spacer has a predetermined height” and “spacers have predetermined inter-spacer distance” means, respectively, that the value of the spacer height and the inter spacer distance is known prior to a CROF process. It is not predetermined, if the value of the spacer height and the inter-spacer distance is not known prior to a CROF process. For example, in the case that beads are sprayed on a plate as spacers, where beads are landed on random locations of the plate, the inter-spacer distance is not predetermined. Another example of not predetermined inter spacer distance is that the spacers moves during a CROF processes.

The term “a spacer is fixed on its respective plate” in a CROF process means that the spacer is attached to a location of a plate and the attachment to that location is maintained during a CROF (i.e. the location of the spacer on respective plate does not change). An example of “a spacer is fixed with its respective plate” is that a spacer is monolithically made of one piece of material of the plate, and the location of the spacer relative to the plate surface does not change during CROF. An example of “a spacer is not fixed with its respective plate” is that a spacer is glued to a plate by an adhesive, but during a use of the plate, during CROF, the adhesive cannot hold the spacer at its original location on the plate surface and the spacer moves away from its original location on the plate surface.

The term “a spacer is fixed to a plate monolithically” means the spacer and the plate behavior like a single piece of an object where, during a use, the spacer does not move or separated from its original location on the plate.

The term “open configuration” of the two plates in a CROF process means a configuration in which the two plates are either partially or completely separated apart and the spacing between the plates is not regulated by the spacers

The term “closed configuration” of the two plates in a CROF process means a configuration in which the plates are facing each other, the spacers and a relevant volume of the sample are between the plates, the thickness of the relevant volume of the sample is regulated by the plates and the spacers, wherein the relevant volume is at least a portion of an entire volume of the sample.

The term “a sample thickness is regulated by the plate and the spacers” in a CROF process means that for a give condition of the plates, the sample, the spacer, and the plate compressing method, the thickness of at least a port of the sample at the closed configuration of the plates can be predetermined from the properties of the spacers and the plate.

The term “inner surface” or “sample surface” of a plate in a CROF device refers to the surface of the plate that touches the sample, while the other surface (that does not touch the sample) of the plate is termed “outer surface”.

The term “X-Plate” of a CROF device refers to a plate that comprises spaces that are on the sample surface of the plate, wherein the spacers have a predetermined inter-spacer distance and spacer height, and wherein at least one of the spacers is inside the sample contact area.

The term “CROF device” refers to a device that performs a CROF process. The term “CROFed” means that a CROF process is used. For example, the term “a sample was CROFed” means that the sample was put inside a CROF device, a CROF process was performed, and the sample was hold, unless stated otherwise, at a final configuration of the CROF.

The term “CROF plates” refers to the two plates used in performing a CROF process.

The term “surface smoothness” or “surface smoothness variation” of a planar surface refers to the average deviation of a planar surface from a perfect flat plane over a short distance that is about or smaller than a few micrometers. The surface smoothness is different from the surface flatness variation. A planar surface can have a good surface flatness, but poor surface smoothness.

The term “surface flatness” or “surface flatness variation” of a planar surface refers to the average deviation of a planar surface from a perfect flat plane over a long distance that is about or larger than 10 um. The surface flatness variation is different from the surface smoothness. A planar surface can have a good surface smoothness, but poor surface flatness (i.e. large surface flatness variation).

The term “relative surface flatness” of a plate or a sample is the ratio of the plate surface flatness variation to the final sample thickness.

The term “final sample thickness” in a CROF process refers to, unless specified otherwise, the thickness of the sample at the closed configuration of the plates in a CORF process.

The term “compression method” in CROF refers to a method that brings two plates from an open configuration to a closed configuration.

The term of “interested area” or “area of interest” of a plate refers to the area of the plate that is relevant to the function that the plates perform.

The term “at most” means “equal to or less than”. For example, a spacer height is at most 1 um, it means that the spacer height is equal to or less than 1 um.

The term “sample area” means the area of the sample in the direction approximately parallel to the space between the plates and perpendicular to the sample thickness.

The term “sample thickness” refers to the sample dimension in the direction normal to the surface of the plates that face each other (e.g., the direction of the spacing between the plates).

The term “plate-spacing” refers to the distance between the inner surfaces of the two plates.

The term “deviation of the final sample thickness” in a CROF means the difference between the predetermined spacer height (determined from fabrication of the spacer) and the average of the final sample thickness, wherein the average final sample thickness is averaged over a given area (e.g. an average of 25 different points (4 mm apart) over 1.6 cm by 1.6 cm area).

The term “uniformity of the measured final sample thickness” in a CROF process means the standard deviation of the measured final sample thickness over a given sample area (e.g. the standard deviation relative to the average).

The term “relevant volume of a sample” and “relevant area of a sample” in a CROF process refers to, respectively, the volume and the area of a portion or entire volume of the sample deposited on the plates during a CROF process, that is relevant to a function to be performed by a respective method or device, wherein the function includes, but not limited to, reduction in binding time of analyte or entity, detection of analytes, quantify of a volume, quantify of a concentration, mixing of reagents, or control of a concentration (analytes, entity or reagents).

The term “some embodiments”, “in some embodiments” “in the present invention, in some embodiments”, “embodiment”, “one embodiment”, “another embodiment”, “certain embodiments”, “many embodiments”, or alike refers, unless specifically stated otherwise, to an embodiment(s) that is (are) applied to the entire disclosure (i.e. the entire invention).

The term “height” or “thickness” of an object in a CROF process refers to, unless specifically stated, the dimension of the object that is in the direction normal to a surface of the plate. For example, spacer height is the dimension of the spacer in the direction normal to a surface of the plate, and the spacer height and the spacer thickness means the same thing.

The term “area” of an object in a CROF process refers to, unless specifically stated, the area of the object that is parallel to a surface of the plate. For example, spacer area is the area of the spacer that is parallel to a surface of the plate.

The term “lateral” or “laterally” in a CROF process refers to, unless specifically stated, the direction that is parallel to a surface of the plate.

The term “width” of a spacer in a CROF process refers to, unless specifically stated, a lateral dimension of the spacer.

The term “a spacer inside a sample” means that the spacer is surrounded by the sample (e.g. a pillar spacer inside a sample).

The term “critical bending span” of a plate in a CROF process refers the span (i.e. distance) of the plate between two supports, at which the bending of the plate, for a given flexible plate, sample, and compression force, is equal to an allowed bending. For example, if an allowed bending is 50 nm and the critical bending span is 40 um for a given flexible plate, sample, and compression force, the bending of the plate between two neighboring spacers 40 um apart will be 50 nm, and the bending will be less than 50 nm if the two neighboring spacers is less than 40 um.

The term “flowable” for a sample means that when the thickness of the sample is reduced, the lateral dimension increases. For an example, a stool sample is regarded flowable.

In some embodiments of the present invention, a sample under a CROF process do not to be flowable to benefit from the process, as long as the sample thickness can be reduced under a CROF process. For an example, to stain a tissue by put a dye on a surface of the CROF plate, a CROF process can reduce the tissue thickness and hence speed up the saturation incubation time for staining by the dye.

The terms “CROF Card (or card)”, “COF Card”, “QMAX-Card”, “Q-Card”, “CROF device”, “COF device”, “QMAX-device”, “CROF plates”, “COF plates”, and “QMAX-plates” are interchangeable, except that in some embodiments, the COF card does not comprise spacers; and the terms refer to a device that comprises a first plate and a second plate that are movable relative to each other into different configurations (including an open configuration and a closed configuration), and that comprises spacers (except some embodiments of the COF) that regulate the spacing between the plates. The term “X-plate” refers to one of the two plates in a CROF card, wherein the spacers are fixed to this plate. More descriptions of the COF Card, CROF Card, and X-plate are described in the provisional application Ser. No. 62/456,065, filed on Feb. 7, 2017, which is incorporated herein in its entirety for all purposes.

Examples of Present Invention I. Formation of Uniform Thin Fluidic Layer by an Imprecise Force Pressing

The term “imprecise pressing force” without adding the details and then adding a definition for imprecise pressing force.

As used herein, the term “imprecise” in the context of a force (e.g. “imprecise pressing force”) refers to a force that

(a) has a magnitude that is not precisely known or precisely predictable at the time the force is applied;

(b) has a magnitude in the range of 1N to 20N and/or a pressure in a range of 0.1 psi to 280 psi;

(c) varies in magnitude from one application of the force to the next; and

(d) the imprecision (i.e. the variation) of the force in (a) and (c) is at least 20% of the total force that actually is applied.

An imprecise force can be applied by human hand, for example, e.g., by pinching an object together between a thumb and index finger, or by pinching and rubbing an object together between a thumb and index finger.

A. Imprecise Force, Specify IGS{circumflex over ( )}4/hE

-   A1. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising:

a first plate, a second plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises an inner surface that has a         sample contact area for contacting a fluidic sample;     -   iv. each of the plates comprises, on its respective outer         surface, a force area for applying an imprecise pressing force         that forces the plates together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, and a         predetermined fixed inter-spacer-distance;     -   vii. the fourth power of the inter-spacer-distance (IDS) divided         by the thickness (h) and the Young's modulus (E) of the flexible         plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less; and     -   viii. at least one of the spacers is inside the sample contact         area;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample is deposited in the open configuration and the plates are forced to the closed configuration by applying the imprecise pressing force on the force area; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers.

-   A2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises an inner surface that has             a sample contact area for contacting a fluidic sample;         -   iv. each of the plates comprises, on its respective outer             surface, a force area for applying an imprecise pressing             force that forces the plates together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, and a             predetermined fixed inter-spacer-distance;         -   vii. the fourth power of the inter-spacer-distance (IDS)             divided by the thickness (h) and the Young's modulus (E) of             the flexible plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less; and         -   viii. at least one of the spacers is inside the sample             contact area;     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.             B. Hand Pressing, Specify Spacer Hardness-Contact Area             Product -   B1. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise force,     comprising:

a first plate, a second plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample;     -   iv. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, a         predetermined width, and a predetermined inter-spacer-distance;     -   vii. a ratio of the inter-spacer-distance to the spacer width is         1.5 or larger; and     -   viii. at least one of the spacers is inside the sample contact         area;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers; and

wherein the force that presses the two plates into the closed configuration is an imprecise pressing force provided by human hand.

-   B2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises, on its respective inner             surface, a sample contact area for contacting and/or             compressing a fluidic sample;         -   iv. each of the plates comprises, on its respective outer             surface, an area for applying a force that forces the plates             together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, a             predetermined width, and a predetermined             inter-spacer-distance;         -   vii. a ratio of the inter-spacer-distance to the spacer             width is 1.5 or larger; and         -   viii. at least one of the spacers is inside the sample             contact area;     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.             C. Hand pressing, Specify IDS/hE & Spacer Hardness-Contact             Area Product -   C1. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise force,     comprising:

a first plate, a second plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample;     -   iv. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, a         predetermined width, and a predetermined inter-spacer-distance;     -   vii. a ratio of the inter-spacer-distance to the spacer width is         1.5 or larger; and     -   viii. at least one of the spacers is inside the sample contact         area;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers;

wherein the force that presses the two plates into the closed configuration is imprecise, and is provided by human hand.

-   C2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises, on its respective inner             surface, a sample contact area for contacting and/or             compressing a fluidic sample;         -   iv. each of the plates comprises, on its respective outer             surface, an area for applying a force that forces the plates             together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, a             predetermined width, and a predetermined             inter-spacer-distance;         -   vii. a ratio of the inter-spacer-distance to the spacer             width is 1.5 or larger; and         -   viii. at least one of the spacers is inside the sample             contact area;     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.             D. Hand Pressing, Specify Pillar Spacer and Ratio of IDS/W -   D1. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise force,     comprising:

a first plate, a second plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample;     -   iv. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, a         predetermined width, and a predetermined inter-spacer-distance;     -   vii. a ratio of the inter-spacer-distance to the spacer width is         1.5 or larger.     -   viii. at least one of the spacers is inside the sample contact         area; and

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers;

wherein the force that presses the two plates into the closed configuration is imprecise, and is provided by human hand.

-   D2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises, on its respective inner             surface, a sample contact area for contacting and/or             compressing a fluidic sample;         -   iv. each of the plates comprises, on its respective outer             surface, an area for applying a force that forces the plates             together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, a             predetermined width, and a predetermined             inter-spacer-distance;         -   vii. a ratio of the inter-spacer-distance to the spacer             width is 1.5 or larger.         -   viii. at least one of the spacers is inside the sample             contact area; and     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.             E. Q (V-1) Volume Determination, Specify IGS{circumflex over             ( )}4/hE -   E1. A device for determining a relevant sample volume by pressing     with an imprecise force provided by human hand, comprising:

a first plate, a second plate, spacers, and an area-determination device, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample that has a relevant volume to be measured;     -   iv. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, and a         predetermined constant inter-spacer-distance;     -   vii. a fourth power of the inter-spacer-distance (IDS) divided         by the thickness (h) and the Young's modulus (E) of the flexible         plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   viii. at least one of the spacers is inside the sample contact         area; and     -   ix. the area-determination device is configured to determine the         lateral area of the relevant volume;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers;

wherein the relevant volume of the sample is a partial or entire volume of the uniform thickness layer and the value of the relevant volume is determined by the uniform thickness and the determined lateral area; and

wherein the force that presses the two plates into the closed configuration is imprecise, and is provided by human hand.

The device of any prior embodiment, wherein the area-determination device is a camera.

The area-determination device comprises an area in the sample contact area of a plate, wherein the area is less than 1/100, 1/20, 1/10, ⅙, ⅕, ¼, ⅓, ½, ⅔ of the sample contact area, or in a range between any of the two values.

The area-determination device comprises a camera and an area in the sample contact area of a plate, wherein the area is in contact with the sample.

-   E2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises, on its respective inner             surface, a sample contact area for contacting and/or             compressing a fluidic sample that has a relevant volume to             be measured;         -   iv. each of the plates comprises, on its respective outer             surface, an area for applying a force that forces the plates             together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, and a             predetermined constant inter-spacer-distance;         -   vii. a fourth power of the inter-spacer-distance (IDS)             divided by the thickness (h) and the Young's modulus (E) of             the flexible plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.         -   viii. at least one of the spacers is inside the sample             contact area; and         -   ix. the area-determination device is configured to determine             the lateral area of the relevant volume;     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.             F. Q (V-1) Volume Determination, Specify IGS{circumflex over             ( )}4/hE -   F1. A device for determining a relevant sample volume by pressing     with an imprecise force provided by human hand, comprising:

a first plate, a second plate, spacers, and area-determination device, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample that has a relevant volume to be measured;     -   iv. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   v. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   vi. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, and a         predetermined constant inter-spacer-distance;     -   vii. a fourth power of the inter-spacer-distance (IDS) divided         by the thickness (h) and the Young's modulus (E) of the flexible         plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   viii. at least one of the spacers is inside the sample contact         area; and     -   ix. the area-determination device is configured to determine the         lateral area of the relevant volume;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers;

wherein the relevant volume of the sample is a partial or entire volume of the uniform thickness layer and the value of the relevant volume is determined by the uniform thickness and the determined lateral area; and

wherein the force that presses the two plates into the closed configuration is imprecise, and is provided by human hand.

-   F2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a first plate, a second plate, and spacers,         wherein:         -   i. the plates are movable relative to each other into             different configurations;         -   ii. one or both plates are flexible;         -   iii. each of the plates comprises, on its respective inner             surface, a sample contact area for contacting and/or             compressing a fluidic sample that has a relevant volume to             be measured;         -   iv. each of the plates comprises, on its respective outer             surface, an area for applying a force that forces the plates             together;         -   v. one or both of the plates comprise the spacers that are             permanently fixed on the inner surface of a respective             plate;         -   vi. the spacers have a predetermined substantially uniform             height that is equal to or less than 200 microns, and a             predetermined constant inter-spacer-distance;         -   vii. a fourth power of the inter-spacer-distance (IDS)             divided by the thickness (h) and the Young's modulus (E) of             the flexible plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.         -   viii. at least one of the spacers is inside the sample             contact area; and         -   ix. the area-determination device is configured to determine             the lateral area of the relevant volume;     -   (b) obtaining a fluidic sample;     -   (c) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), using the two plates to compress at least part of         the sample into a layer of substantially uniform thickness that         is confined by the sample contact surfaces of the plates,         wherein the uniform thickness of the layer is regulated by the         spacers and the plates, wherein the compressing comprises:         -   bringing the two plates together; and         -   conformable pressing, either in parallel or sequentially, an             area of at least one of the plates to press the plates             together to a closed configuration, wherein the conformable             pressing generates a substantially uniform pressure on the             plates over the at least part of the sample, and the             pressing spreads the at least part of the sample laterally             between the sample contact surfaces of the plates, and             wherein the closed configuration is a configuration in which             the spacing between the plates in the layer of uniform             thickness region is regulated by the spacers; and wherein             the reduced thickness of the sample reduces the time for             mixing the reagents on the storage site with the sample, and         -   wherein the force that presses the two plates into the             closed configuration is an imprecise pressing force provided             by human hand.     -   1. The device or method of any prior embodiment, wherein spacers         have a flat top.     -   2. The device or method of any prior embodiment, wherein the         device is further configured to have, after the pressing force         is removed, a sample thickness that is substantially the same in         thickness and uniformity as that when the force is applied.     -   3. The device or method of any prior embodiment, wherein the         imprecise force is provided by human hand.     -   4. The device or method of any prior embodiment, wherein the         inter spacer distance is substantially constant.     -   5. The device or method of any prior embodiment, wherein the         inter spacer distance is substantially periodic in the area of         the uniform sample thickness area.     -   6. The device or method of any prior embodiment, wherein the         multiplication product of the filling factor and the Young's         modulus of the spacer is 2 MPa or larger.     -   The device or method of any prior embodiment, wherein the force         is applied by hand directly or indirectly.     -   8. The device or method of any prior embodiment, wherein the         force applied is in the range of 5 N to 20 N.     -   9. The device or method of any prior embodiment wherein the         highly uniform layer has a thickness that varies by less than         15%, 10%, or 5% of an average thickness.     -   10. The device or method of any prior embodiment, wherein the         imprecise force is applied by pinching the device between a         thumb and forefinger.     -   11. The device or method of any prior embodiment, wherein the         predetermined sample thickness is larger than the spacer height.     -   12. The device or method of any prior embodiment, wherein the         device holds itself in the closed configuration after the         pressing force has been removed.     -   13. The device or method of any prior embodiment, wherein the         uniform thickness sample layer area is larger than that area         upon which the pressing force is applied.     -   14. The device or method of any prior embodiment, wherein the         spacers do not significantly deform during application of the         pressing force.     -   15. The device or method of any prior embodiment, wherein the         pressing force is not predetermined beforehand and is not         measured.     -   16. The device of any prior device embodiment, wherein the         analyte comprises a molecule (e.g., a protein, peptides, DNA,         RNA, nucleic acid, or other molecule), cells, tissues, viruses,         and nanoparticles with different shapes.     -   17. The device of any prior device embodiment, wherein the         analyte comprises white blood cells, red blood cells and         platelets.     -   18. The device of any prior device embodiment, wherein the         analyte is stained.     -   19. The method or device of any prior embodiment, wherein the         inter spacer distance (SD) is equal or less than about 120 um         (micrometer).     -   20. The method or device of any prior embodiment, wherein the         inter spacer distance (SD) is equal or less than about 100 um         (micrometer).     -   21. The method or device of any prior embodiment, wherein the         fourth power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   22. The method or device of any prior embodiment, wherein the         fourth power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁵ um³/GPa or less.     -   23. The method or device of any prior embodiment, wherein the         spacers have pillar shape, a substantially flat top surface, a         predetermined substantially uniform height, and a predetermined         constant inter-spacer distance that is at least about 2 times         larger than the size of the analyte, wherein the Young's modulus         of the spacers times the filling factor of the spacers is equal         or larger than 2 MPa, wherein the filling factor is the ratio of         the spacer contact area to the total plate area, and wherein,         for each spacer, the ratio of the lateral dimension of the         spacer to its height is at least 1 (one).     -   24. The method or device of any prior embodiment, wherein the         spacers have pillar shape, a substantially flat top surface, a         predetermined substantially uniform height, and a predetermined         constant inter-spacer distance that is at least about 2 times         larger than the size of the analyte, wherein the Young's modulus         of the spacers times the filling factor of the spacers is equal         or larger than 2 MPa, wherein the filling factor is the ratio of         the spacer contact area to the total plate area, and wherein,         for each spacer, the ratio of the lateral dimension of the         spacer to its height is at least 1 (one), wherein the fourth         power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   25. The device of any prior device embodiment, wherein the ratio         of the inter-spacing distance of the spacers to the average         width of the spacer is 2 or larger, and the filling factor of         the spacers multiplied by the Young's modulus of the spacers is         2 MPa or larger.     -   26. The method or device of any prior embodiment, wherein the         analytes is the analyte in 5 detection of proteins, peptides,         nucleic acids, synthetic compounds, and inorganic compounds.     -   27. The method or device of any prior embodiment, wherein the         sample is a biological sample selected from amniotic fluid,         aqueous humour, vitreous humour, blood (e.g., whole blood,         fractionated blood, plasma or serum), breast milk, cerebrospinal         fluid (CSF), cerumen (earwax), chyle, chime, endolymph,         perilymph, feces, breath, gastric acid, gastric juice, lymph,         mucus (including nasal drainage and phlegm), pericardial fluid,         peritoneal fluid, pleural fluid, pus, rheum, saliva, exhaled         breath condensates, sebum, semen, sputum, sweat, synovial fluid,         tears, vomit, and urine.     -   28. The method or device of any prior embodiment, wherein the         spacers have a shape of pillars and a ratio of the width to the         height of the pillar is equal or larger than one.     -   29. The method of any prior embodiment, wherein the sample that         is deposited on one or both of the plates has an unknown volume.     -   30. The method or device of any prior embodiment, wherein the         samples is for the detection, purification and quantification of         chemical compounds or biomolecules that correlates with the         stage of certain diseases.     -   31. The method or device of any prior embodiment, wherein the         samples is related to infectious and parasitic disease,         injuries, cardiovascular disease, cancer, mental disorders,         neuropsychiatric disorders, pulmonary diseases, renal diseases,         and other and organic diseases.     -   32. The method or device of any prior embodiment, wherein the         samples is related to the detection, purification and         quantification of microorganism.     -   33. The method or device of any prior embodiment, wherein the         samples is related to virus, fungus and bacteria from         environment, e.g., water, soil, or biological samples.     -   34. The method or device of any prior embodiment, wherein the         samples is related to the detection, quantification of chemical         compounds or biological samples that pose hazard to food safety         or national security, e.g. toxic waste, anthrax.     -   35. The method or device of any prior embodiment, wherein the         samples is related to quantification of vital parameters in         medical or physiological monitor.     -   36. The method or device of any prior embodiment, wherein the         samples is related to glucose, blood, oxygen level, total blood         count.     -   37. The method or device of any prior embodiment, wherein the         samples is related to the detection and quantification of         specific DNA or RNA from biosamples.     -   38. The method or device of any prior embodiment, wherein the         samples is related to the sequencing and comparing of genetic         sequences in DNA in the chromosomes and mitochondria for genome         analysis.     -   39. The method or device of any prior embodiment, wherein the         samples is related to detect reaction products, e.g., during         synthesis or purification of pharmaceuticals.     -   40. The method or device of any prior embodiment, wherein the         samples is cells, tissues, bodily fluids, and stool.     -   41. The method or device of any prior embodiment, wherein the         sample is the sample in the detection of proteins, peptides,         nucleic acids, synthetic compounds, inorganic compounds.     -   42. The method or device of any prior embodiment, wherein the         sample is the sample in the fields of human, veterinary,         agriculture, foods, environments, and drug testing.     -   43. The method or device of any prior embodiment, wherein the         sample is a biological sample is selected from blood, serum,         plasma, a nasal swab, a nasopharyngeal wash, saliva, urine,         gastric fluid, spinal fluid, tears, stool, mucus, sweat, earwax,         oil, a glandular secretion, cerebral spinal fluid, tissue,         semen, vaginal fluid, interstitial fluids derived from tumorous         tissue, ocular fluids, spinal fluid, a throat swab, breath,         hair, finger nails, skin, biopsy, placental fluid, amniotic         fluid, cord blood, lymphatic fluids, cavity fluids, sputum, pus,         microbiota, meconium, breast milk, exhaled condensate         nasopharyngeal wash, throat swab, stool samples, hair, finger         nail, ear wax, breath, connective tissue, muscle tissue, nervous         tissue, epithelial tissue, cartilage, cancerous sample, or bone.     -   44. The devices or methods of any prior embodiment, wherein the         spacers regulating the layer of uniform thickness have a filling         factor of at least 1%, wherein the filling factor is the ratio         of the spacer area in contact with the layer of uniform         thickness to the total plate area in contact with the layer of         uniform thickness.         Flat Top of Pillar Spacers

In certain embodiments of the present invention, the spacers are pillars that have a flat top and a foot fixed on one plate, wherein the flat top has a smoothness with a small surface variation, and the variation is less than 5, 10 nm, 20 nm, 30 nm, 50 nm, 100 nm, 200 nm, 300 nm, 400 nm, 500 nm, 600 nm, 700 nm, 800 nm, 1000 nm, or in a range between any two of the values. A preferred flat pillar top smoothness is that surface variation of 50 nm or less.

Furthermore, the surface variation is relative to the spacer height and the ratio of the pillar flat top surface variation to the spacer height is less than 0.5%, 1%, 3%, 5%, 7%, 10%, 15%, 20%, 30%, 40%, or in a range between any two of the values. A preferred flat pillar top smoothness has a ratio of the pillar flat top surface variation to the spacer height is less than 2%, 5%, or 10%.

Sidewall Angle of Pillar Spacers

In certain embodiments of the present invention, the spacers are pillars that have a sidewall angle. In some embodiments, the sidewall angle is less than 5 degree (measured from the normal of a surface), 10 degree, 20 degree, 30 degree, 40 degree, 50 degree, 70 degree, or in a range between any two of the values. In a preferred embodiment, the sidewall angle is less 5 degree, 10 degree, or 20 degree.

Formation of Uniform Thin Fluidic Layer by an Imprecise Force Pressing

In certain embodiment of the present invention, a uniform thin fluidic sample layer is formed by using a pressing with an imprecise force. The term “imprecise pressing force” without adding the details and then adding a definition for imprecise pressing force. As used herein, the term “imprecise” in the context of a force (e.g. “imprecise pressing force”) refers to a force that

(a) has a magnitude that is not precisely known or precisely predictable at the time the force is applied; (b) has a pressure in the range of 0.01 kg/cm² (centimeter square) to 100 kg/cm², (c) varies in magnitude from one application of the force to the next; and (d) the imprecision (i.e. the variation) of the force in (a) and (c) is at least 20% of the total force that actually is applied.

An imprecise force can be applied by human hand, for example, e.g., by pinching an object together between a thumb and index finger, or by pinching and rubbing an object together between a thumb and index finger.

In some embodiments, the imprecise force by the hand pressing has a pressure of 0.01 kg/cm2, 0.1 kg/cm2, 0.5 kg/cm2, 1 kg/cm2, 2 kg/cm2, kg/cm2, 5 kg/cm2, 10 kg/cm2, 20 kg/cm2, 30 kg/cm2, 40 kg/cm2, 50 kg/cm2, 60 kg/cm2, 100 kg/cm2, 150 kg/cm2, 200 kg/cm2, or a range between any two of the values; and a preferred range of 0.1 kg/cm2 to 0.5 kg/cm2, 0.5 kg/cm2 to 1 kg/cm2, 1 kg/cm2 to 5 kg/cm2, 5 kg/cm2 to 10 kg/cm2 (Pressure).

Spacer Filling Factor.

The term “spacer filling factor” or “filling factor” refers to the ratio of the spacer contact area to the total plate area”, wherein the spacer contact area refers, at a closed configuration, the contact area that the spacer's top surface contacts to the inner surface of a plate, and the total plate area refers the total area of the inner surface of the plate that the flat top of the spacers contact. Since there are two plates and each spacer has two contact surfaces each contacting one plate, the filling fact is the filling factor of the smallest.

For example, if the spacers are pillars with a flat top of a square shape (10 um×10 um), a nearly uniform cross-section and 2 um tall, and the spacers are periodic with a period of 100 um, then the filing factor of the spacer is 1%. If in the above example, the foot of the pillar spacer is a square shape of 15 um×15 um, then the filling factor is still 1% by the definition.

IDS{circumflex over ( )}4/hE

-   A1. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing, comprising:

a first plate, a second plate, and spacers, wherein:

-   -   ix. the plates are movable relative to each other into different         configurations;     -   x. one or both plates are flexible;     -   xi. each of the plates comprises an inner surface that has a         sample contact area for contacting a fluidic sample;     -   xii. each of the plates comprises, on its respective outer         surface, a force area for applying an pressing force that forces         the plates together;     -   xiii. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   xiv. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, and a         predetermined fixed inter-spacer-distance;     -   xv. the fourth power of the inter-spacer-distance (ISD) divided         by the thickness (h) and the Young's modulus (E) of the flexible         plate (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less; and     -   xvi. at least one of the spacers is inside the sample contact         area;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample is deposited in the open configuration and the plates are forced to the closed configuration by applying the pressing force on the force area; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers.

-   A2. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing, comprising the steps of:     -   (e) obtaining a device of embodiment A1;     -   (f) depositing a fluidic sample on one or both of the plates;         when the plates are configured in an open configuration, wherein         the open configuration is a configuration in which the two         plates are partially or completely separated apart and the         spacing between the plates is not regulated by the spacers;     -   (g) after (b), forcing the two plates into a closed         configuration, in which: at least part of the sample is         compressed by the two plates into a layer of substantially         uniform thickness, wherein the uniform thickness of the layer is         confined by the sample contact surfaces of the plates and is         regulated by the plates and the spacers. -   A3. A device for analyzing a fluidic sample, comprising:

a first plate, a second plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates has, on its respective inner surface, a         sample contact area for contacting a fluidic sample,     -   iv. one or both of the plates comprise the spacers and the         spacers are fixed on the inner surface of a respective plate;     -   v. the spacers have a predetermined substantially uniform height         that is equal to or less than 200 microns, and the         inter-spacer-distance is predetermined;     -   vi. the Young's modulus of the spacers multiplied by the filling         factor of the spacers is at least 2 MPa; and     -   vii. at least one of the spacers is inside the sample contact         area; and

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates; and

wherein another of the configurations is a closed configuration which is configured after the sample is deposited in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness, wherein the uniform thickness of the layer is confined by the sample contact surfaces of the plates and is regulated by the plates and the spacers.

-   A4. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing, comprising the steps of:     -   (a) obtaining a device of embodiment A3;     -   (b) depositing a fluidic sample on one or both of the plates;         when the plates are configured in an open configuration, wherein         the open configuration is a configuration in which the two         plates are partially or completely separated apart and the         spacing between the plates is not regulated by the spacers;     -   (c) after (b), forcing the two plates into a closed         configuration, in which: at least part of the sample is         compressed by the two plates into a layer of substantially         uniform thickness, wherein the uniform thickness of the layer is         confined by the sample contact surfaces of the plates and is         regulated by the plates and the spacers. -   A5. A device for analyzing a fluidic sample, comprising:

a first plate and a second plate, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates has, on its respective surface, a sample         contact area for contacting a sample that contains an analyte,     -   iv. one or both of the plates comprise spacers that are         permanently fixed to a plate within a sample contact area,         wherein the spacers have a predetermined substantially uniform         height and a predetermined fixed inter-spacer distance that is         at least about 2 times larger than the size of the analyte, up         to 200 urn, and wherein at least one of the spacers is inside         the sample contact area;

wherein one of the configurations is an open configuration, in which: the two plates are separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates; and

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness, wherein the uniform thickness of the layer is confined by the sample contact surfaces of the plates and is regulated by the plates and the spacers.

-   A6. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing, comprising the steps of:     -   (a) obtaining a device of embodiment A5;     -   (b) depositing a fluidic sample on one or both of the plates;         when the plates are configured in an open configuration, wherein         the open configuration is a configuration in which the two         plates are partially or completely separated apart and the         spacing between the plates is not regulated by the spacers;     -   (c) after (b), forcing the two plates into a closed         configuration, in which: at least part of the sample is         compressed by the two plates into a layer of substantially         uniform thickness, wherein the uniform thickness of the layer is         confined by the sample contact surfaces of the plates and is         regulated by the plates and the spacers. -   A7. A device for forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing, comprising:

a first plate, a second plate, and spacers, wherein:

-   -   ix. the plates are movable relative to each other into different         configurations;     -   x. one or both plates are flexible;     -   xi. each of the plates comprises, on its respective inner         surface, a sample contact area for contacting and/or compressing         a fluidic sample;     -   xii. each of the plates comprises, on its respective outer         surface, an area for applying a force that forces the plates         together;     -   xiii. one or both of the plates comprise the spacers that are         permanently fixed on the inner surface of a respective plate;     -   xiv. the spacers have a predetermined substantially uniform         height that is equal to or less than 200 microns, a         predetermined width, and a predetermined fixed         inter-spacer-distance;     -   xv. a ratio of the inter-spacer-distance to the spacer width is         1.5 or larger; and     -   xvi. at least one of the spacers is inside the sample contact         area;

wherein one of the configurations is an open configuration, in which: the two plates are partially or completely separated apart, the spacing between the plates is not regulated by the spacers, and the sample is deposited on one or both of the plates;

wherein another of the configurations is a closed configuration which is configured after the sample deposition in the open configuration; and in the closed configuration: at least part of the sample is compressed by the two plates into a layer of highly uniform thickness and is substantially stagnant relative to the plates, wherein the uniform thickness of the layer is confined by the sample contact areas of the two plates and is regulated by the plates and the spacers.

-   A8. A method of forming a thin fluidic sample layer with a uniform     predetermined thickness by pressing with an imprecise pressing     force, comprising the steps of:     -   (a) obtaining a device of embodiment A7;     -   (b) obtaining a fluidic sample;     -   (e) depositing the sample on one or both of the plates; when the         plates are configured in an open configuration, wherein the open         configuration is a configuration in which the two plates are         partially or completely separated apart and the spacing between         the plates is not regulated by the spacers;     -   (d) after (c), forcing the two plates into a closed         configuration, in which: at least part of the sample is         compressed by the two plates into a layer of substantially         uniform thickness, wherein the uniform thickness of the layer is         confined by the sample contact surfaces of the plates and is         regulated by the plates and the spacers.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate and a flat top surface for contacting the other plate.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate, a flat top surface for contacting the other plate, substantially uniform cross-section.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate and a flat top surface for contacting the other plate, wherein the flat top surface of the pillars has a variation in less than 10 nm.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate and a flat top surface for contacting the other plate, wherein the flat top surface of the pillars has a variation in less than 50 nm.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate and a flat top surface for contacting the other plate, wherein the flat top surface of the pillars has a variation in less than 50 nm.

The devices or methods of any prior embodiment, wherein the spacers have a shape of pillar with a foot fixed on one of the plate and a flat top surface for contacting the other plate, wherein the flat top surface of the pillars has a variation in less than 10 nm, 20 nm, 30 nm, 100 nm, 200 nm, or in a range of any two of the values.

The devices or methods of any prior embodiment, wherein the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 2 MPa.

The devices or methods of any prior embodiment, wherein the sample comprises an analyte and the predetermined constant inter-spacer distance is at least about 2 times larger than the size of the analyte, up to 200 um.

The devices or methods of any prior embodiment, wherein the sample comprise an analyte, the predetermined constant inter-spacer distance is at least about 2 times larger than the size of the analyte, up to 200 um, and the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 2 MPa.

The devices or methods of any prior embodiment, wherein a fourth power of the inter-spacer-distance (IDS) divided by the thickness (h) and the Young's modulus (E) of the flexible plate (ISD{circumflex over ( )}4/(hE)) is 5×10{circumflex over ( )}6 um{circumflex over ( )}3/GPa or less.

The devices or methods of any prior embodiment, wherein a fourth power of the inter-spacer-distance (IDS) divided by the thickness (h) and the Young's modulus (E) of the flexible plate (ISD{circumflex over ( )}4/(hE)) is 1×10{circumflex over ( )}6 um{circumflex over ( )}3/GPa or less.

The devices or methods of any prior embodiment, wherein a fourth power of the inter-spacer-distance (IDS) divided by the thickness (h) and the Young's modulus (E) of the flexible plate (ISD{circumflex over ( )}4/(hE)) is 5×10{circumflex over ( )}5 um{circumflex over ( )}3/GPa or less.

The devices or methods of any prior embodiment, wherein the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 2 MPa, and a fourth power of the inter-spacer-distance (IDS) divided by the thickness (h) and the Young's modulus (E) of the flexible plate (ISD{circumflex over ( )}4/(hE)) is 1×10{circumflex over ( )}5 um{circumflex over ( )}3/GPa or less.

The devices or methods of any prior embodiment, wherein the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 2 MPa, and a fourth power of the inter-spacer-distance (IDS) divided by the thickness (h) and the Young's modulus (E) of the flexible plate (ISD{circumflex over ( )}4/(hE)) is 1×10{circumflex over ( )}4 um″3/GPa or less.

The devices or methods of any prior embodiment, wherein the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 20 MPa.

The devices or methods of any prior embodiment, wherein the ratio of the inter-spacing distance of the spacers to the average width of the spacer is 2 or larger.

The devices or methods of any prior embodiment, wherein the ratio of the inter-spacing distance of the spacers to the average width of the spacer is 2 or larger, and the Young's modulus of the spacers multiplied by the filling factor of the spacers is at least 2 MPa.

The devices or methods of any prior embodiment, wherein inter-spacer distance that is at least about 2 times larger than the size of the analyte, up to 200 um.

The devices or methods of any prior embodiment, wherein a ratio of the inter-spacer-distance to the spacer width is 1.5 or larger.

The devices or methods of any prior embodiment, wherein a ratio of the width to the height of the spacer is 1 or larger.

The devices or methods of any prior embodiment, wherein a ratio of the width to the height of the spacer is 1.5 or larger.

The devices or methods of any prior embodiment, wherein a ratio of the width to the height of the spacer is 2 or larger.

The devices or methods of any prior embodiment, wherein a ratio of the width to the height of the spacer is larger than 2, 3, 5, 10, 20, 30, 50, or in a range of any two the value.

The methods of any prior embodiment, wherein the force that presses the two plates into the closed configuration is an imprecise pressing force.

The methods of any prior embodiment, wherein the force that presses the two plates into the closed configuration is an imprecise pressing force provided by human hand.

The methods of any prior embodiment, wherein the forcing of the two plates to compress at least part of the sample into a layer of substantially uniform thickness comprises a use of a conformable pressing, either in parallel or sequentially, an area of at least one of the plates to press the plates together to a closed configuration, wherein the conformable pressing generates a substantially uniform pressure on the plates over the at least part of the sample, and the pressing spreads the at least part of the sample laterally between the sample contact surfaces of the plates, and wherein the closed configuration is a configuration in which the spacing between the plates in the layer of uniform thickness region is regulated by the spacers; and wherein the reduced thickness of the sample reduces the time for mixing the reagents on the storage site with the sample.

The methods of any prior embodiment, wherein the pressing force is an imprecise force that has a magnitude which is, at the time that the force is applied, either (a) unknown and unpredictable, or (b) cannot be known and cannot be predicted within an accuracy equal or better than 20% of the average pressing force applied.

The methods of any prior embodiment, wherein the pressing force is an imprecise force that has a magnitude which is, at the time that the force is applied, either (a) unknown and unpredictable, or (b) cannot be known and cannot be predicted within an accuracy equal or better than 30% of the average pressing force applied.

The methods of any prior embodiment, wherein the pressing force is an imprecise force that has a magnitude which is, at the time that the force is applied, either (a) unknown and unpredictable, or (b) cannot be known and cannot be predicted within an accuracy equal or better than 30% of the average pressing force applied; and wherein the layer of highly uniform thickness has a variation in thickness uniform of 20% or less.

The methods of any prior embodiment, wherein the pressing force is an imprecise force that has a magnitude which cannot, at the time that the force is applied, be determined within an accuracy equal or better than 30%, 40%, 50%, 70%, 100%, 200%, 300%, 500%, 1000%, 2000%, or in a range between any of the two values.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of in the range of 10 um to 200 um.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of in the range of 20 um to 100 um.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of in the range of 25 um to 180 um.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of in the range of 200 um to 260 um.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of equal to or less than 250 um, 225 um, 200 um, 175 um, 150 um, 125 um, 100 um, 75 um, 50 um, 25 um, 10 um, 5 um, 1 um, or in a range between the two of the values.

The devices or methods of any prior method, wherein the sample has a viscosity in the range of 0.1 to 4 (mPa s).

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness of in the range of 200 um to 260 um.

The devices or methods of any prior embodiment, wherein the flexible plate has a thickness in the range of 20 um to 200 um and Young's modulus in the range 0.1 to 5 GPa.

-   -   45. The method of any prior claim, wherein the sample deposition         of step (b) is a deposition directly from a subject to the plate         without using any transferring devices.     -   46. The method any prior claim, wherein during the deposition of         step (b), the amount of the sample deposited on the plate is         unknown.     -   47. The method of any prior claim, wherein the method further         comprises an analyzing step (e) that analyze the sample.     -   48. The method of any prior claim, wherein the analyzing         step (e) comprises calculating the volume of a relevant sample         volume by measuring the lateral area of the relevant sample         volume and calculating the volume from the lateral area and the         predetermined spacer height.     -   49. The method of any prior claim, wherein the analyzing         step (e) comprises measuring:         -   i. imaging, illuminescence selected from photoluminescence,             electroluminescence, and electrochemiluminescence,         -   iii. surface Raman scattering,         -   iv. electrical impedance selected from resistance,             capacitance, and inductance, or         -   v. any combination of i-iv.     -   50. The method of any prior claim, wherein the analyzing         step (e) comprises reading, image analysis, or counting of the         analyte, or a combination of thereof.     -   51. The method of any prior claim, wherein the sample contains         one or plurality of analytes, and one or both plate sample         contact surfaces comprise one or a plurality of binding sites         that each binds and immobilize a respective analyte.     -   52. The method of any prior claim, wherein one or both plate         sample contact surfaces comprise one or a plurality of storage         sites that each stores a reagent or reagents, wherein the         reagent(s) dissolve and diffuse in the sample during or after         step (c).     -   53. The method of any prior claim, wherein one or both plate         sample contact surfaces comprises one or a plurality of         amplification sites that are each capable of amplifying a signal         from the analyte or a label of the analyte when the analyte or         label is within 500 nm from an amplification site.     -   54. The method of any prior claim, wherein:         -   i. one or both plate sample contact surfaces comprise one or             a plurality of binding sites that each binds and immobilize             a respective analyte; or         -   ii. one or both plate sample contact surfaces comprise, one             or a plurality of storage sites that each stores a reagent             or reagents; wherein the reagent(s) dissolve and diffuse in             the sample during or after step (c), and wherein the sample             contains one or plurality of analytes; or         -   iii. one or a plurality of amplification sites that are each             capable of amplifying a signal from the analyte or a label             of the analyte when the analyte or label is 500 nm from the             amplification site; or         -   iv. any combination of i to iii.     -   55. The devices or methods of any prior embodiment, wherein the         liquid sample is a biological sample selected from amniotic         fluid, aqueous humour, vitreous humour, blood (e.g., whole         blood, fractionated blood, plasma or serum), breast milk,         cerebrospinal fluid (CSF), cerumen (earwax), chyle, chime,         endolymph, perilymph, feces, breath, gastric acid, gastric         juice, lymph, mucus (including nasal drainage and phlegm),         pericardial fluid, peritoneal fluid, pleural fluid, pus, rheum,         saliva, exhaled breath condensates, sebum, semen, sputum, sweat,         synovial fluid, tears, vomit, and urine.     -   56. The devices or methods of any prior embodiment, wherein the         layer of uniform thickness in the closed configuration is less         than 150 um.     -   57. The method of any prior claim, wherein the pressing is         provided by a pressured liquid, a pressed gas, or a conformal         material.     -   58. The method of any prior claim, wherein the analyzing         comprises counting cells in the layer of uniform thickness.     -   59. The method of any prior claim, wherein the analyzing         comprises performing an assay in the layer of uniform thickness.     -   60. The devices or methods of any prior embodiment, wherein the         assay is a binding assay or biochemical assay.     -   61. The method of any prior claim, wherein the sample deposited         has a total volume less 0.5 uL     -   62. The method of any prior claim, wherein multiple drops of         sample are deposited onto one or both of the plates.     -   63. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 1 □m to 120 □m.     -   64. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 120 □m to 50 □m.     -   65. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 120 □m to 200 □m.     -   66. The device of any prior device claim, wherein the flexible         plates have a thickness in the range of 20 um to 250 um and         Young's modulus in the range 0.1 to 5 GPa.     -   67. The device of any prior device claim, wherein for a flexible         plate, the thickness of the flexible plate times the Young's         modulus of the flexible plate is in the range 60 to 750 GPa-um.     -   68. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         at least 1 mm².     -   69. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         at least 3 mm².     -   70. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         at least 5 mm².     -   71. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         at least 10 mm².     -   72. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         at least 20 mm².     -   73. The device of any prior device claim, wherein the layer of         uniform thickness sample is uniform over a lateral area that is         in a range of 20 mm² to 100 mm².     -   74. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +/−5% or better.     -   75. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +1-10% or better.     -   76. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +/−20% or better.     -   77. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +/−30% or better.     -   78. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +/−40% or better.     -   79. The device of any prior device claim, wherein the layer of         uniform thickness sample has a thickness uniformity of up to         +/−50% or better.     -   80. The device of any prior device claim, wherein the spacers         are pillars with a cross-sectional shape selected from round,         polygonal, circular, square, rectangular, oval, elliptical, or         any combination of the same.     -   81. The device of any prior device claim, wherein the spacers         have pillar shape, have a substantially flat top surface, and         have substantially uniform cross-section, wherein, for each         spacer, the ratio of the lateral dimension of the spacer to its         height is at least 1.     -   82. The device of any prior device claim, wherein the inter         spacer distance is periodic.     -   83. The device of any prior device claim, wherein the spacers         have a filling factor of 1% or higher, wherein the filling         factor is the ratio of the spacer contact area to the total         plate area.     -   84. The device of any prior device claim, wherein the Young's         modulus of the spacers times the filling factor of the spacers         is equal or larger than 20 MPa, wherein the filling factor is         the ratio of the spacer contact area to the total plate area.     -   85. The device of any prior device claim, wherein the spacing         between the two plates at the closed configuration is in less         200 um.     -   86. The device of any prior device claim, wherein the spacing         between the two plates at the closed configuration is a value         selected from between 1.8 um and 3.5 um.     -   87. The device of any prior device claim, wherein the spacing         are fixed on a plate by directly embossing the plate or         injection molding of the plate.     -   88. The device of any prior device claim, wherein the materials         of the plate and the spacers are selected from polystyrene,         PMMA, PC, COC, COP, or another plastic.     -   89. The device of any prior device claim, wherein the spacers         have a pillar shape, and the sidewall corners of the spacers         have a round shape with a radius of curvature at least 1 □M.     -   90. The device of any prior device claim, wherein the spacers         have a density of at least 1000/mm².     -   91. The device of any prior device claim, wherein at least one         of the plates is transparent.     -   92. The device of any prior device claim, wherein the mold used         to make the spacers is fabricated by a mold containing features         that are fabricated by either (a) directly reactive ion etching         or ion beam etched or (b) by a duplication or multiple         duplication of the features that are reactive ion etched or ion         beam etched.     -   93. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is in the         range of 1% to 5%.

The devices or methods of any prior embodiment, wherein the surface variation is relative to the spacer height and the ratio of the pillar flat top surface variation to the spacer height is less than 0.5%, 1%, 3%, 5%, 7%, 10%, 15%, 20%, 30%, 40%, or in a range between any two of the values. A preferred flat pillar top smoothness has a ratio of the pillar flat top surface variation to the spacer height is less than 2%, 5%, or 10%.

-   -   94. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is in the         range of 1% to 5%.     -   95. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is in the         range of 5% to 10%.     -   96. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is in the         range of 10% to 20%.     -   97. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is in the         range of 20% to 30%.     -   98. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is 5%, 10%,         20%, 30%, 40%, 50%, or in a range of any two of the values.     -   99. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor is 50%,         60%, 70%, 80%, or in a range of any two of the values.     -   100. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 2 MPa and         10 MPa.     -   101. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 10 MPa and         20 MPa.     -   102. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 20 MPa and         40 MPa.     -   103. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 40 MPa and         80 MPa.     -   104. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 80 MPa and         120 MPa.     -   105. The devices or methods of any prior embodiment, wherein the         spacers are configured, such that the filling factor multiplies         the Young's modulus of the spacer is in the range of 120 MPa to         150 MPa.     -   106. The devices or methods of any prior embodiment, wherein the         device further comprises a dry reagent coated on one or both         plates.     -   107. The devices or methods of any prior embodiment, wherein the         device further comprises, on one or both plates, a dry binding         site that has a predetermined area, wherein the dry binding site         binds to and immobilizes an analyte in the sample.     -   108. The devices or methods of any prior embodiment, wherein the         device further comprises, on one or both plates, a releasable         dry reagent and a release time control material that delays the         time that the releasable dry regent is released into the sample.     -   109. The device of any prior embodiment, wherein the release         time control material delays the time that the dry regent starts         is released into the sample by at least 3 seconds.     -   110. The device of any prior embodiment, wherein the regent         comprises anticoagulant and/or staining reagent(s)     -   111. The device of any prior embodiment, wherein the reagent         comprises cell lysing reagent(s)     -   112. The devices or methods of any prior embodiment, wherein the         device further comprises, on one or both plates, one or a         plurality of dry binding sites and/or one or a plurality of         reagent sites.     -   113. The device of any prior device embodiment, wherein the         analyte comprises a molecule (e.g., a protein, peptides, DNA,         RNA, nucleic acid, or other molecule), cells, tissues, viruses,         and nanoparticles with different shapes.     -   114. The device of any prior device embodiment, wherein the         analyte comprises white blood cells, red blood cells and         platelets.     -   115. The device of any prior device embodiment, wherein the         analyte is stained.     -   116. The devices or methods of any prior embodiment, wherein the         spacers regulating the layer of uniform thickness have a filling         factor of at least 1%, wherein the filling factor is the ratio         of the spacer area in contact with the layer of uniform         thickness to the total plate area in contact with the layer of         uniform thickness.     -   117. The devices or methods of any prior embodiment, wherein for         spacers regulating the layer of uniform thickness, the Young's         modulus of the spacers times the filling factor of the spacers         is equal or larger than 10 MPa, wherein the filling factor is         the ratio of the spacer area in contact with the layer of         uniform thickness to the total plate area in contact with the         layer of uniform thickness.     -   118. The devices or methods of any prior embodiment, wherein for         a flexible plate, the thickness of the flexible plate times the         Young's modulus of the flexible plate is in the range 60 to 750         GPa-um.     -   119. The devices or methods of any prior embodiment, wherein for         a flexible plate, the fourth power of the inter-spacer-distance         (ISD) divided by the thickness of the flexible plate (h) and the         Young's modulus (E) of the flexible plate, ISD⁴/(hE), is equal         to or less than 10⁶ um³/GPa,     -   120. The devices or methods of any prior embodiment, wherein one         or both plates comprises a location marker, either on a surface         of or inside the plate, that provide information of a location         of the plate.     -   121. The devices or methods of any prior embodiment, wherein one         or both plates comprises a scale marker, either on a surface of         or inside the plate, that provide information of a lateral         dimension of a structure of the sample and/or the plate.     -   122. The devices or methods of any prior embodiment, wherein one         or both plates comprises an imaging marker, either on surface of         or inside the plate, that assists an imaging of the sample.     -   123. The devices or methods of any prior embodiment, wherein the         spacers functions as a location marker, a scale marker, an         imaging marker, or any combination of thereof.     -   124. The devices or methods of any prior embodiment, wherein the         average thickness of the layer of uniform thickness is about         equal to a minimum dimension of an analyte in the sample.     -   125. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 7 □m to 50 □m.     -   126. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 50 □m to 120 □m.     -   127. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 120 □m to 200 □m         (micron).     -   128. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is substantially periodic.     -   129. The devices or methods of any prior embodiment, wherein the         spacers are pillars with a cross-sectional shape selected from         round, polygonal, circular, square, rectangular, oval,         elliptical, or any combination of the same.     -   130. The devices or methods of any prior embodiment, wherein the         spacers have are pillar shape and have a substantially flat top         surface, wherein, for each spacer, the ratio of the lateral         dimension of the spacer to its height is at least 1.     -   131. The devices or methods of any prior embodiment, wherein         each spacer has the ratio of the lateral dimension of the spacer         to its height is at least 1.     -   132. The devices or methods of any prior embodiment, wherein the         minimum lateral dimension of spacer is less than or         substantially equal to the minimum dimension of an analyte in         the sample.     -   133. The devices or methods of any prior embodiment, wherein the         minimum lateral dimension of spacer is in the range of 0.5 um to         100 um.     -   134. The devices or methods of any prior embodiment, wherein the         minimum lateral dimension of spacer is in the range of 0.5 um to         10 um.     -   135. The devices or methods of any prior embodiment, wherein the         sample is blood.     -   136. The devices or methods of any prior embodiment, wherein the         sample is whole blood without dilution by liquid.     -   137. The devices or methods of any prior embodiment, wherein the         sample is a biological sample selected from amniotic fluid,         aqueous humour, vitreous humour, blood (e.g., whole blood,         fractionated blood, plasma or serum), breast milk, cerebrospinal         fluid (CSF), cerumen (earwax), chyle, chime, endolymph,         perilymph, feces, breath, gastric acid, gastric juice, lymph,         mucus (including nasal drainage and phlegm), pericardial fluid,         peritoneal fluid, pleural fluid, pus, rheum, saliva, exhaled         breath condensates, sebum, semen, sputum, sweat, synovial fluid,         tears, vomit, and urine.     -   138. The devices or methods of any prior embodiment, wherein the         sample is a biological sample, an environmental sample, a         chemical sample, or clinical sample.     -   139. The devices or methods of any prior embodiment, wherein the         spacers have a pillar shape, and the sidewall corners of the         spacers have a round shape with a radius of curvature at least 1         □m.     -   140. The devices or methods of any prior embodiment, wherein the         spacers have a density of at least 100/mm².     -   141. The devices or methods of any prior embodiment, wherein the         spacers have a density of at least 1000/mm².     -   142. The devices or methods of any prior embodiment, wherein at         least one of the plates is transparent.     -   143. The devices or methods of any prior embodiment, wherein at         least one of the plates is made from a flexible polymer.     -   144. The devices or methods of any prior embodiment, wherein,         for a pressure that compresses the plates, the spacers are not         compressible and/or, independently, only one of the plates is         flexible.     -   145. The device of any of any prior embodiment, wherein the         flexible plate has a thickness in the range of 10 um to 200 um.     -   146. The devices or methods of any prior embodiment, wherein the         variation is less than 30%.     -   147. The devices or methods of any prior embodiment, wherein the         variation is less than 10%.     -   148. The devices or methods of any prior embodiment, wherein the         variation is less than 5%.     -   149. The devices or methods of any prior embodiment, wherein the         first and second plates are connected and are configured to be         changed from the open configuration to the closed configuration         by folding the plates.     -   150. The devices or methods of any prior embodiment, wherein the         first and second plates are connected by a hinge and are         configured to be changed from the open configuration to the         closed configuration by folding the plates along the hinge.     -   151. The devices or methods of any prior embodiment, wherein the         first and second plates are connected by a hinge that is a         separate material to the plates, and are configured to be         changed from the open configuration to the closed configuration         by folding the plates along the hinge     -   152. The devices or methods of any prior embodiment, wherein the         first and second plates are made in a single piece of material         and are configured to be changed from the open configuration to         the closed configuration by folding the plates.     -   153. The devices or methods of any prior embodiment, wherein the         layer of uniform thickness sample is uniform over a lateral area         that is at least 1 mm².     -   154. The devices or methods of any prior embodiment, wherein the         device is configured to analyze the sample in 60 seconds or         less.     -   155. The devices or methods of any prior embodiment, wherein at         the closed configuration, the final sample thickness device is         configured to analyze the sample in 60 seconds or less.     -   156. The devices or methods of any prior embodiment, wherein at         the closed configuration, the final sample thickness device is         configured to analyze the sample in 10 seconds or less.     -   157. The devices or methods of any prior embodiment, wherein the         dry binding site comprises a capture agent.     -   158. The devices or methods of any prior embodiment, wherein the         dry binding site comprises an antibody or nucleic acid.     -   159. The devices or methods of any prior embodiment, wherein the         releasable dry reagent is a labeled reagent.     -   160. The devices or methods of any prior embodiment, wherein the         releasable dry reagent is a fluorescently-labeled reagent.     -   161. The devices or methods of any prior embodiment, wherein the         releasable dry reagent is a fluorescently-labeled antibody.     -   162. The devices or methods of any prior embodiment, wherein the         releasable dry reagent is a cell stain.     -   163. The devices or methods of any prior embodiment, wherein the         releasable dry reagent is a cell lysing.     -   164. The devices or methods of any prior embodiment, wherein the         detector is an optical detector that detects an optical signal.     -   165. The devices or methods of any prior embodiment, wherein the         detector is an electric detector that detect electrical signal.     -   166. The device of any prior device embodiment, wherein the         spacing are fixed on a plate by directly embossing the plate or         injection molding of the plate.     -   167. The device of any prior device embodiment, wherein the         materials of the plate and the spacers are selected from         polystyrene, PMMA, PC, COC, COP, or another plastic.     -   168. A system for rapidly analyzing a sample using a mobile         phone comprising:         -   (a) a device of any prior embodiment;         -   (b) a mobile communication device comprising:             -   i. one or a plurality of cameras for the detecting                 and/or imaging the sample;             -   ii. electronics, signal processors, hardware and                 software for receiving and/or processing the detected                 signal and/or the image of the sample and for remote                 communication; and         -   (c) a light source from either the mobile communication             device or an external source;         -   wherein the detector in the devices or methods of any prior             embodiment is provided by the mobile communication device,             and detects an analyte in the sample at the closed             configuration.     -   169. The system of any prior system embodiment, wherein one of         the plates has a binding site that binds an analyte, wherein at         least part of the uniform sample thickness layer is over the         binding site, and is substantially less than the average lateral         linear dimension of the binding site.     -   170. The system of any prior system embodiment, further         comprising:         -   (d) a housing configured to hold the sample and to be             mounted to the mobile communication device.     -   171. The system of any prior system embodiment, wherein the         housing comprises optics for facilitating the imaging and/or         signal processing of the sample by the mobile communication         device, and a mount configured to hold the optics on the mobile         communication device.     -   172. The system of any prior system embodiment, wherein an         element of the optics in the housing is movable relative to the         housing.     -   173. The system of any prior system embodiment, wherein the         mobile communication device is configured to communicate test         results to a medical professional, a medical facility or an         insurance company.     -   174. The system of any prior system embodiment, wherein the         mobile communication device is further configured to communicate         information on the test and the subject with the medical         professional, medical facility or insurance company.     -   175. The system of any prior system embodiment, wherein the         mobile communication device is further configured to communicate         information of the test to a cloud network, and the cloud         network process the information to refine the test results.     -   176. The system of any prior system embodiment, wherein the         mobile communication device is further configured to communicate         information of the test and the subject to a cloud network, the         cloud network process the information to refine the test         results, and the refined test results will send back the         subject.     -   177. The system of any prior system embodiment, wherein the         mobile communication device is configured to receive a         prescription, diagnosis or a recommendation from a medical         professional.     -   178. The system of any prior system embodiment, wherein the         mobile communication device is configured with hardware and         software to:         -   (a) capture an image of the sample;         -   (b) analyze a test location and a control location in in             image; and         -   (c) compare a value obtained from analysis of the test             location to a threshold value that characterizes the rapid             diagnostic test.     -   179. The system of any prior system embodiment, wherein at least         one of the plates comprises a storage site in which assay         reagents are stored.     -   180. The system of any prior system embodiment, at least one of         the cameras reads a signal from the device.     -   181. The system of any prior system embodiment, wherein the         mobile communication device communicates with the remote         location via a wifi or cellular network.     -   182. The system of any prior system embodiment, wherein the         mobile communication device is a mobile phone.     -   183. A method for rapidly analyzing an analyte in a sample using         a mobile phone, comprising:         -   (a) depositing a sample on the device of any prior system             embodiment;         -   (b) assaying an analyte in the sample deposited on the             device to generate a result; and         -   (c) communicating the result from the mobile communication             device to a location remote from the mobile communication             device.     -   184. The method of any prior embodiments embodiment, wherein the         analyte comprises a molecule (e.g., a protein, peptides, DNA,         RNA, nucleic acid, or other molecule), cells, tissues, viruses,         and nanoparticles with different shapes.     -   185. The method of any prior embodiment, wherein the analyte         comprises white blood cell, red blood cell and platelets.     -   186. The method of any prior embodiment, wherein the assaying         comprises performing a white blood cells differential assay.     -   187. The method of any prior embodiments embodiment, wherein the         method comprises:         -   analyzing the results at the remote location to provide an             analyzed result; and         -   communicating the analyzed result from the remote location             to the mobile communication device.     -   188. The method of any prior embodiment, wherein the analysis is         done by a medical professional at a remote location.     -   189. The method of any prior embodiment, wherein the mobile         communication device receives a prescription, diagnosis or a         recommendation from a medical professional at a remote location.     -   190. The method of any prior embodiment, wherein the sample is a         bodily fluid.     -   191. The method of any prior embodiment, wherein the bodily         fluid is blood, saliva or urine.     -   192. The method of any prior embodiment, wherein the sample is         whole blood without dilution by a liquid.     -   193. The method of any prior embodiment, wherein the assaying         step comprises detecting an analyte in the sample.     -   194. The method of any prior embodiment, wherein the analyte is         a biomarker.     -   195. The method of any prior embodiment, wherein the analyte is         a protein, nucleic acid, cell, or metabolite.     -   196. The method of any prior embodiment, wherein the method         comprises counting the number of red blood cells.     -   197. The method of any of any prior embodiment, wherein the         method comprises counting the number of white blood cells.     -   198. The method of any prior embodiment, wherein method         comprises staining the cells in the sample and counting the         number of neutrophils, lymphocytes, monocytes, eosinophils and         basophils.     -   199. The method of any prior embodiments embodiment, wherein the         assay done in step (b) is a binding assay or a biochemical         assay.     -   200. A method for analyzing a sample comprising:         -   obtaining a device of any prior device embodiment;         -   depositing the sample onto one or both pates of the device;         -   placing the plates in a closed configuration and applying an             external force over at least part of the plates; and         -   analyzing the in the layer of uniform thickness while the             plates are the closed configuration.     -   201. The devices or methods of any prior embodiment, wherein the         first plate further comprises, on its surface, a first         predetermined assay site and a second predetermined assay site,         wherein the distance between the edges of the assay site is         substantially larger than the thickness of the uniform thickness         layer when the plates are in the closed position, wherein at         least a part of the uniform thickness layer is over the         predetermined assay sites, and wherein the sample has one or a         plurality of analytes that are capable of diffusing in the         sample.     -   202. The devices or methods of any prior embodiment, wherein the         first plate has, on its surface, at least three analyte assay         sites, and the distance between the edges of any two neighboring         assay sites is substantially larger than the thickness of the         uniform thickness layer when the plates are in the closed         position, wherein at least a part of the uniform thickness layer         is over the assay sites, and wherein the sample has one or a         plurality of analytes that are capable of diffusing in the         sample.     -   203. The devices or methods of any prior embodiment, wherein the         first plate has, on its surface, at least two neighboring         analyte assay sites that are not separated by a distance that is         substantially larger than the thickness of the uniform thickness         layer when the plates are in the closed position, wherein at         least a part of the uniform thickness layer is over the assay         sites, and wherein the sample has one or a plurality of analytes         that are capable of diffusing in the sample.     -   204. The devices or methods of any prior embodiment, wherein the         analyte assay area is between a pair of electrodes.     -   205. The devices or methods of any prior embodiment, wherein the         assay area is defined by a patch of dried reagent.     -   206. The devices or methods of any prior embodiment, wherein the         assay area binds to and immobilizes the analyte     -   207. The devices or methods of any prior embodiment, wherein the         assay area is defined by a patch of binding reagent that, upon         contacting the sample, dissolves into the sample, diffuses in         the sample, and binds to the analyte.     -   208. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 14 □m to 200 □m.     -   209. The devices or methods of any prior embodiment, wherein the         inter-spacer distance is in the range of 7 □m to 20 □m.     -   210. The devices or methods of any prior embodiment, wherein the         spacers are pillars with a cross-sectional shape selected from         round, polygonal, circular, square, rectangular, oval,         elliptical, or any combination of the same.     -   211. The devices or methods of any prior embodiment, wherein the         spacers have a pillar shape and have a substantially flat top         surface, wherein, for each spacer, the ratio of the lateral         dimension of the spacer to its height is at least 1.     -   212. The devices or methods of any prior embodiment, wherein the         spacers have a pillar shape, and the sidewall corners of the         spacers have a round shape with a radius of curvature at least 1         □m.     -   213. The devices or methods of any prior embodiment, wherein the         spacers have a density of at least 1000/mm².     -   214. The devices or methods of any prior embodiment, wherein at         least one of the plates is transparent.     -   215. The devices or methods of any prior embodiment, wherein at         least one of the plates is made from a flexible polymer.     -   216. The devices or methods of any prior embodiment, wherein         only one of the plates is flexible.         The device of any prior embodiment, wherein the         area-determination device is a camera.

The area-determination device comprises an area in the sample contact area of a plate, wherein the area is less than 1/100, 1/20, 1/10, ⅙, ⅕, ¼, ⅓, ½, ⅔ of the sample contact area, or in a range between any of the two values.

The area-determination device comprises a camera and an area in the sample contact area of a plate, wherein the area is in contact with the sample.

The devices or methods of any prior embodiment, wherein the deformable sample comprises a liquid sample.

The devices or methods of any prior embodiment, wherein the imprecision force has a variation at least 30% of the total force that actually is applied.

The devices or methods of any prior embodiment, wherein the imprecision force has a variation at least 20%, 30%, 40%, 50%, 60, 70%, 80%, 90% 100%, 150%, 200%, 300%, 500%, or in a range of any two values, of the total force that actually is applied.

-   -   217. The device or method of any prior embodiment, wherein         spacers have a flat top.     -   218. The device or method of any prior embodiment, wherein the         device is further configured to have, after the pressing force         is removed, a sample thickness that is substantially the same in         thickness and uniformity as that when the force is applied.     -   219. The device or method of any prior embodiment, wherein the         imprecise force is provided by human hand.     -   220. The device or method of any prior embodiment, wherein the         inter spacer distance is substantially constant.     -   221. The device or method of any prior embodiment, wherein the         inter spacer distance is substantially periodic in the area of         the uniform sample thickness area.     -   222. The device or method of any prior embodiment, wherein the         multiplication product of the filling factor and the Young's         modulus of the spacer is 2 MPa or larger.     -   223. The device or method of any prior embodiment, wherein the         force is applied by hand directly or indirectly.     -   224. The device or method of any prior embodiment, wherein the         force applied is in the range of 5 N to 20 N.     -   225. The device or method of any prior embodiment wherein the         highly uniform layer has a thickness that varies by less than         15%, 10%, or 5% of an average thickness.     -   226. The device or method of any prior embodiment, wherein the         imprecise force is applied by pinching the device between a         thumb and forefinger.     -   227. The device or method of any prior embodiment, wherein the         predetermined sample thickness is larger than the spacer height.     -   228. The device or method of any prior embodiment, wherein the         device holds itself in the closed configuration after the         pressing force has been removed.     -   229. The device or method of any prior embodiment, wherein the         uniform thickness sample layer area is larger than that area         upon which the pressing force is applied.     -   230. The device or method of any prior embodiment, wherein the         spacers do not significantly deform during application of the         pressing force.     -   231. The device or method of any prior embodiment, wherein the         pressing force is not predetermined beforehand and is not         measured.     -   232. The device of any prior device embodiment, wherein the         analyte comprises a molecule (e.g., a protein, peptides, DNA,         RNA, nucleic acid, or other molecule), cells, tissues, viruses,         and nanoparticles with different shapes.     -   233. The device of any prior device embodiment, wherein the         analyte comprises white blood cells, red blood cells and         platelets.     -   234. The device of any prior device embodiment, wherein the         analyte is stained.     -   235. The method or device of any prior embodiment, wherein the         inter spacer distance (SD) is equal or less than about 120 um         (micrometer).     -   236. The method or device of any prior embodiment, wherein the         inter spacer distance (SD) is equal or less than about 100 um         (micrometer).     -   237. The method or device of any prior embodiment, wherein the         fourth power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   238. The method or device of any prior embodiment, wherein the         fourth power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁵ um³/GPa or less.     -   239. The method or device of any prior embodiment, wherein the         spacers have pillar shape, a substantially flat top surface, a         predetermined substantially uniform height, and a predetermined         constant inter-spacer distance that is at least about 2 times         larger than the size of the analyte, wherein the Young's modulus         of the spacers times the filling factor of the spacers is equal         or larger than 2 MPa, wherein the filling factor is the ratio of         the spacer contact area to the total plate area, and wherein,         for each spacer, the ratio of the lateral dimension of the         spacer to its height is at least 1 (one).     -   240. The method or device of any prior embodiment, wherein the         spacers have pillar shape, a substantially flat top surface, a         predetermined substantially uniform height, and a predetermined         constant inter-spacer distance that is at least about 2 times         larger than the size of the analyte, wherein the Young's modulus         of the spacers times the filling factor of the spacers is equal         or larger than 2 MPa, wherein the filling factor is the ratio of         the spacer contact area to the total plate area, and wherein,         for each spacer, the ratio of the lateral dimension of the         spacer to its height is at least 1 (one), wherein the fourth         power of the inter-spacer-distance (ISD) divided by the         thickness (h) and the Young's modulus (E) of the flexible plate         (ISD⁴/(hE)) is 5×10⁶ um³/GPa or less.     -   241. The device of any prior device embodiment, wherein the         ratio of the inter-spacing distance of the spacers to the         average width of the spacer is 2 or larger, and the filling         factor of the spacers multiplied by the Young's modulus of the         spacers is 2 MPa or larger.     -   242. The method or device of any prior embodiment, wherein the         analytes is the analyte in 5 detection of proteins, peptides,         nucleic acids, synthetic compounds, and inorganic compounds.     -   243. The method or device of any prior embodiment, wherein the         sample is a biological sample selected from amniotic fluid,         aqueous humour, vitreous humour, blood (e.g., whole blood,         fractionated blood, plasma or serum), breast milk, cerebrospinal         fluid (CSF), cerumen (earwax), chyle, chime, endolymph,         perilymph, feces, breath, gastric acid, gastric juice, lymph,         mucus (including nasal drainage and phlegm), pericardial fluid,         peritoneal fluid, pleural fluid, pus, rheum, saliva, exhaled         breath condensates, sebum, semen, sputum, sweat, synovial fluid,         tears, vomit, and urine.     -   244. The method or device of any prior embodiment, wherein the         spacers have a shape of pillars and a ratio of the width to the         height of the pillar is equal or larger than one.     -   245. The method of any prior embodiment, wherein the sample that         is deposited on one or both of the plates has an unknown volume.     -   246. The method or device of any prior embodiment, wherein the         samples is for the detection, purification and quantification of         chemical compounds or biomolecules that correlates with the         stage of certain diseases.     -   247. The method or device of any prior embodiment, wherein the         samples is related to infectious and parasitic disease,         injuries, cardiovascular disease, cancer, mental disorders,         neuropsychiatric disorders, pulmonary diseases, renal diseases,         and other and organic diseases.     -   248. The method or device of any prior embodiment, wherein the         samples is related to the detection, purification and         quantification of microorganism.     -   249. The method or device of any prior embodiment, wherein the         samples is related to virus, fungus and bacteria from         environment, e.g., water, soil, or biological samples.     -   250. The method or device of any prior embodiment, wherein the         samples is related to the detection, quantification of chemical         compounds or biological samples that pose hazard to food safety         or national security, e.g. toxic waste, anthrax.     -   251. The method or device of any prior embodiment, wherein the         samples is related to quantification of vital parameters in         medical or physiological monitor.     -   252. The method or device of any prior embodiment, wherein the         samples is related to glucose, blood, oxygen level, total blood         count.     -   253. The method or device of any prior embodiment, wherein the         samples is related to the detection and quantification of         specific DNA or RNA from biosamples.     -   254. The method or device of any prior embodiment, wherein the         samples is related to the sequencing and comparing of genetic         sequences in DNA in the chromosomes and mitochondria for genome         analysis.     -   255. The method or device of any prior embodiment, wherein the         samples is related to detect reaction products, e.g., during         synthesis or purification of pharmaceuticals.     -   256. The method or device of any prior embodiment, wherein the         samples is cells, tissues, bodily fluids, and stool.     -   257. The method or device of any prior embodiment, wherein the         sample is the sample in the detection of proteins, peptides,         nucleic acids, synthetic compounds, inorganic compounds.     -   258. The method or device of any prior embodiment, wherein the         sample is the sample in the fields of human, veterinary,         agriculture, foods, environments, and drug testing.     -   259. The method or device of any prior embodiment, wherein the         sample is a biological sample is selected from blood, serum,         plasma, a nasal swab, a nasopharyngeal wash, saliva, urine,         gastric fluid, spinal fluid, tears, stool, mucus, sweat, earwax,         oil, a glandular secretion, cerebral spinal fluid, tissue,         semen, vaginal fluid, interstitial fluids derived from tumorous         tissue, ocular fluids, spinal fluid, a throat swab, breath,         hair, finger nails, skin, biopsy, placental fluid, amniotic         fluid, cord blood, lymphatic fluids, cavity fluids, sputum, pus,         microbiota, meconium, breast milk, exhaled condensate         nasopharyngeal wash, throat swab, stool samples, hair, finger         nail, ear wax, breath, connective tissue, muscle tissue, nervous         tissue, epithelial tissue, cartilage, cancerous sample, or bone.     -   260. The devices or methods of any prior embodiment, wherein the         spacers regulating the layer of uniform thickness have a filling         factor of at least 1%, wherein the filling factor is the ratio         of the spacer area in contact with the layer of uniform         thickness to the total plate area in contact with the layer of         uniform thickness.         Manufacturing of Q-Card         MA1. An embodiment of the Q-Card comprising: a first plate, a         second plate, and a hinge, wherein     -   i. the first plate, that is about 200 nm to 1500 nm thick,         comprises, on its inner surface, (a) a sample contact area for         contacting a sample, and (b) a sample overflow dam that         surrounds the sample contact area is configured to present a         sample flow outside of the dam;     -   ii. the second plate is 10 um to 250 um thick and comprises, on         its inner surface, (a) a sample contact area for contacting a         sample, and (b) spacers on the sample contact area;     -   iii. the hinge that connect the first and the second plates; and         wherein the first and second plate are movable relative to each         other around the axis of the hinge.         MA2. An embodiment of the Q-Card comprising: a first plate, a         second plate, and a hinge, wherein     -   i. the first plate, that is about 200 nm to 1500 nm thick,         comprises, on its inner surface, (a) a sample contact area for         contacting a sample, (b) a sample overflow dam that surrounds         the sample contact area is configured to present a sample flow         outside of the dam, and (c) spacers on the sample contact area;     -   ii. the second plate, that is 10 urn to 250 urn thick,         comprises, on its inner surface, a sample contact area for         contacting a sample;     -   iii. the hinge that connect the first and the second plates; and         wherein the first and second plate are movable relative to each         other around the axis of the hinge.         MA3. An embodiment of the Q-Card comprising: a first plate, a         second plate, and a hinge, wherein     -   i. the first plate, that is about 200 nm to 1500 nm thick,         comprises, on its inner surface, (a) a sample contact area for         contacting a sample, and (b) spacers on the sample contact area;     -   ii. the second plate, that is 10 urn to 250 urn thick,         comprises, on its inner surface, (a) a sample contact area for         contacting a sample, and (b) a sample overflow dam that         surrounds the sample contact area is configured to present a         sample flow outside of the dam, and;     -   iii. the hinge that connect the first and the second plates; and         wherein the first and second plate are movable relative to each         other around the axis of the hinge.         MA4 An embodiment of the Q-Card comprising: a first plate, a         second plate, and a hinge, wherein     -   i. the first plate, that is about 200 nm to 1500 nm thick,         comprises, on its inner surface, a sample contact area for         contacting a sample;     -   ii. the second plate, that is 10 urn to 250 urn thick,         comprises, on its inner surface, (a) a sample contact area for         contacting a sample, (b) a sample overflow dam that surrounds         the sample contact area is configured to present a sample flow         outside of the dam, and (c) spacers on the sample contact area;         and     -   iii. the hinge that connect the first and the second plates; and         wherein the first and second plate are movable relative to each         other around the axis of the hinge.         M1 An embodiment of a method for fabricating the Q-Card of any         embodiments of MA1 to MA4, comprising:

(a) injection molding of the first plate,

(b) nanoimprinting or extrusion printing of the second plate.

M2 An embodiment of a method for fabricating the Q-Card of any embodiments of MA1 to MA4, comprising:

(a) Laser cutting the first plate,

(b) nanoimprinting or extrusion printing of the second plate.

M3 An embodiment of a method for fabricating the Q-Card of any embodiments of MA1 to MA4, comprising:

(a) Injection molding and laser cutting the first plate,

(b) nanoimprinting or extrusion printing of the second plate.

M4 An embodiment of a method for fabricating the Q-Card of any embodiments of MA1 to MA4, comprising: nanoimprinting or extrusion printing to fabricated both the first and the second plate.

M5 An embodiment of a method for fabricating the Q-Card of any embodiments of MA1 to MA4, comprising: fabricating the first plate or the second plate, using injection molding, laser cutting the first plate, nanoimprinting, extrusion printing, or a combination of thereof. The method of any embodiments of M1-M5, wherein the method further comprises a step of attach the hinge on the first and the second plates after the fabrication of the first and second plates.

Device and System for Collecting and Analyzing Vapor Condensate, Particularly Exhaled Breath Condensate, as Well Method of Using the Same

A device is provided herein for collecting and analyzing vapor condensate (VC) sample, comprising:

a collection plate, a cover plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates has, on its respective inner surface, a         sample contact area for contacting a vapor condensate (VC)         sample that contains an analyte;     -   iv. the spacers are fixed to the respective inner surface of one         or both of the plates, and have a predetermined substantially         uniform height and a predetermined constant inter-spacer         distance and wherein at least one of the spacers is inside the         sample contact area;         -   wherein one of the configurations is an open configuration,             in which: the two plates are either completely or partially             separated apart, the spacing between the plates is not             regulated by the spacers, and the VC sample is deposited on             one or both of the plates; and         -   wherein another of the configurations is a closed             configuration which is configured after the VC sample             deposition in the open configuration; and in the closed             configuration: at least a part of the VC sample is between             the two plates and in contact with the two plates, and has a             highly uniform thickness that is regulated by the spacers             and the two sample surfaces of the plates and is equal to or             less than 30 □m with a small variation.

Another device is provided herein for collecting and analyzing vapor condensate (VC) sample, comprising:

a collection plate and a cover plate, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible; and     -   iii. each of the plates has, on its respective surface, a sample         contact area for contacting a vapor condensate (VC) sample that         contains an analyte;         -   wherein one of the configurations is an open configuration,             in which: the two plates are either completely or partially             separated apart, and the VC sample is deposited on one or             both of the plates; and         -   wherein another of the configurations is a closed             configuration which is configured after the VC sample             deposition in the open configuration; and in the closed             configuration: at least a part of the VC sample is between             the two plates and in contact with the two plates, and has a             thickness that is regulated by the plate spacing.

In some embodiments, the device further comprises, on one or both plates, one or a plurality of dry binding sites and/or one or a plurality of reagent sites. In some embodiments, the sample is exhale breath condensate.

In some embodiments, the sample is a vapor from a biological sample, an environmental sample, a chemical sample, or clinical sample. In some embodiments, wherein the analyte comprises a molecule (e.g., a protein, peptides, DNA, RNA, nucleic acid, or other molecules), cells, tissues, viruses, and nanoparticles with different shapes. In some embodiments, wherein the analyte comprises volatile organic compounds (VOCs). In some embodiments, wherein the analyte comprises nitrogen, oxygen, CO2, H2O, and inert gases. In some embodiments, wherein the analyte is stained.

In some embodiments, the device may comprise a dry reagent coated on one or both of the plates. In some embodiments, the dry reagent may bind to an analyte in the blood an immobilize the analyte on a surface on one or both of the plates. In these embodiments, the reagent may be an antibody or other specific binding agent, for example. This dry reagent may have a pre-determined area. In other embodiments, the device may comprise a releasable dry reagent on one or more of the plates, e.g., a labeled reagent such as a cell stain or a labeled detection agent such as an antibody or the like. In some cases, there may be a release time control material on the plate that contains the releasable dry reagent, wherein the release time control material delays the time that the releasable dry regent is released into the blood sample.

In some cases, the release time control material delays the time that the dry regent is released into the blood sample by at least 3 seconds, e.g., at least 5 seconds or at least 10 seconds. Some embodiments, the drive may contain multiple dry binding sites and/or multiple reagent sites, thereby allowing multiplex assays to be performed. In some cases, the areas occupied by the drying binding sites may oppose the areas occupied by the reagent sites when the plates are in the closed position.

In some embodiments, the regent comprises labeling or staining reagent(s).

In some embodiments, the spacers regulating the layer of uniform thickness (i.e., the spacers that are spacing the plates away from each other in the layer) have a “filling factor” of at least 1%, e.g., at least 2% or at least 5%, wherein the filling factor is the ratio of the spacer area that is in contact with the layer of uniform thickness to the total plate area that is in contact with the layer of uniform thickness. In some embodiments, for spacers regulating the layer of uniform thickness, the Young's modulus of the spacers times the filling factor of the spacers is equal or larger than 10 MPa, e.g., at least 15 MPa or at least 20 MPa, where the filling factor is the ratio of the spacer area that is in contact with the layer of uniform thickness to the total plate area that is in contact with the layer of uniform thickness. In some embodiments, the thickness of the flexible plate times the Young's modulus of the flexible plate is in the range 60 to 750 GPa-um, e.g., 100 to 300 GPa-um, 300 to 550 GPa-um, or 550 to 750 GPa-um. In some embodiments, for a flexible plate, the fourth power of the inter-spacer-distance (ISD) divided by the thickness of the flexible plate (h) and the Young's modulus (E) of the flexible plate, ISD4/(hE), is equal to or less than 106 um3/GPa, e.g., less than 105 um3/GPa, less than 104 um3/GPa or less than 103 um3/GPa.

In some embodiments, one or both plates comprises a location marker either on a surface of or inside the plate, that provide information of a location of the plate, e.g., a location that is going to be analyzed or a location onto which the blood should be deposited. In some cases, one or both plates may comprise a scale marker, either on a surface of or inside the plate, that provides information of a lateral dimension of a structure of the blood sample and/or the plate. In some embodiments, one or both plates comprises an imaging marker, either on surface of or inside the plate that assists an imaging of the sample. For example, the imaging marker could help focus the imaging device or direct the imaging device to a location on the device. In some embodiments, the spacers can function as a location marker, a scale marker, an imaging marker, or any combination of thereof.

In some embodiments, on one of the sample surface, it further comprises an enclosure-spacer that encloses a partial or entire VC samples deposited on the collection plate.

In some embodiments, the highly uniform thickness has a value equal to or less than 0.5 um. In some embodiments, the highly uniform thickness has a value in the range of 0.5 um to 1 um, 1 um to 2 um, 2 um to 10 um, 10 um to 20 um or 20 um to 30 um.

In some embodiments, the thickness of the at least a part of VC sample at the closed configuration is larger than the thickness of VC sample deposited on the collection plate at an open configuration.

In some embodiments, the thickness of the at least a part of VC sample at the closed configuration is less than the thickness of VC sample deposited on the collection plate at an open configuration.

In some embodiments, wherein the spacers are fixed on a plate by directly embossing the plate or injection molding of the plate.

In some embodiments, wherein the materials of the plate and the spacers are selected from polystyrene, PMMA, PC, COC, COP, or another plastic.

In some embodiments, the inter-spacer spacing in the range of 1 um to 50 um, 50 um to 100 um, 100 um to 200 um or 200 um to 1000 um.

In some embodiments, the VC sample is an exhaled breath condensate from a human or an animal.

In some embodiments, the spacers regulating the layer of uniform thickness have a filling factor of at least 1%, wherein the filling factor is the ratio of the spacer area in contact with the layer of uniform thickness to the total plate area in contact with the layer of uniform thickness.

In some embodiments, for spacers regulating the layer of uniform thickness, the Young's modulus of the spacers times the filling factor of the spacers is equal or larger than 10 MPa, wherein the filling factor is the ratio of the spacer area in contact with the layer of uniform thickness to the total plate area in contact with the layer of uniform thickness.

In some embodiments, for a flexible plate, the thickness of the flexible plate times the Young's modulus of the flexible plate is in the range 60 to 750 GPa-um.

In some embodiments, for a flexible plate, the fourth power of the inter-spacer-distance (ISD) divided by the thickness of the flexible plate (h) and the Young's modulus (E) of the flexible plate, ISD4/(hE), is equal to or less than 106 um3/GPa,

In some embodiments, one or both plates comprises a location marker, either on a surface of or inside the plate, that provide information of a location of the plate.

In some embodiments, one or both plates comprises a scale marker, either on a surface of or inside the plate, that provide information of a lateral dimension of a structure of the sample and/or the plate.

In some embodiments, one or both plates comprises an imaging marker, either on surface of or inside the plate, that assists an imaging of the sample.

In some embodiments, the spacers functions as a location marker, a scale marker, an imaging marker, or any combination of thereof.

In some embodiments, the average thickness of the layer of uniform thickness is about equal to a minimum dimension of an analyte in the sample.

In some embodiments, the inter-spacer distance is 1 μm or less, 5 μm or less, 7 μm or less, 10 μm or less, 20 μm or less, 30 μm or less, 40 μm or less, 50 μm or less, 60 μm or less, 70 μm or less, 80 μm or less, 90 μm or less, 100 μm or less, 200 μm or less, 300 μm or less, 400 μm or less, or in a range between any two of the values.

In some embodiments, the inter-spacer distance is substantially periodic.

In some embodiments, the inter-spacer distance is aperiodic.

In some embodiments, the spacers are pillars with a cross-sectional shape selected from round, polygonal, circular, square, rectangular, oval, elliptical, or any combination of the same.

In some embodiments, the spacers have are pillar shape and have a substantially flat top surface, wherein, for each spacer, the ratio of the lateral dimension of the spacer to its height is at least 1.

In some embodiments, each spacer has the ratio of the lateral dimension of the spacer to its height is at least 1.

In some embodiments, the minimum lateral dimension of spacer is less than or substantially equal to the minimum dimension of an analyte in the sample.

In some embodiments, the minimum lateral dimension of spacer is in the range of 0.5 um to 100 um.

In some embodiments, the minimum lateral dimension of spacer is in the range of 0.5 um to 10 um.

In some embodiments, the spacers have a density of at least 100/mm2. In some embodiments, the spacers have a density of at least 1000/mm2. In some embodiments, at least one of the plates is transparent.

In some embodiments, at least one of the plates is made from a flexible polymer.

In some embodiments, for a pressure that compresses the plates, the spacers are not compressible and/or, independently, only one of the plates is flexible.

In some embodiments, the flexible plate has a thickness in the range of 10 um to 200 um (e.g. about 10 um, 25 um, 50 um, 75 um, 100 um, 125 um, 150 um, 175 um).

In some embodiments, the variation is less than 30%, 10%, 5%, 3% or 1%.

In some embodiments, the first and second plates are connected and are configured to be changed from the open configuration to the closed configuration by folding the plates.

In some embodiments, the first and second plates are connected by a hinge and are configured to be changed from the open configuration to the closed configuration by folding the plates along the hinge.

In some embodiments, the first and second plates are connected by a hinge that is a separate material to the plates, and are configured to be changed from the open configuration to the closed configuration by folding the plates along the hinge

In some embodiments, the first and second plates are made in a single piece of material and are configured to be changed from the open configuration to the closed configuration by folding the plates.

In some embodiments, the layer of uniform thickness sample is uniform over a lateral area that is at least 100 um².

In some embodiments, the layer of uniform thickness sample is uniform over a lateral area that is at least 1 mm².

In some embodiments, the device is configured to analyze the sample in 60 seconds or less.

In some embodiments, at the closed configuration, the final sample thickness device is configured to analyze the sample in 60 seconds or less.

In some embodiments, the device further comprises, on one or both of the plates, one or a plurality of amplification sites that are each capable of amplifying a signal from the analyte or a label of the analyte when the analyte or label is within 500 nm from an amplification site.

In some embodiments, at the closed configuration, the final sample thickness device is configured to analyze the sample in 10 seconds or less.

In some embodiments, the dry binding site comprises a capture agent.

In some embodiments, the dry binding site comprises an antibody or nucleic acid. In some embodiments, the releasable dry reagent is a labeled reagent. In some embodiments, the releasable dry reagent is a fluorescently-labeled reagent. In some embodiments, the releasable dry reagent is a dye. In some embodiments, the releasable dry reagent is a beads. In some embodiments, the releasable dry reagent is a quantum dot. In some embodiments, the releasable dry reagent is a fluorescently-labeled antibody.

In some embodiments, the first plate further comprises, on its surface, a first predetermined assay site and a second predetermined assay site, wherein the distance between the edges of the assay site is substantially larger than the thickness of the uniform thickness layer when the plates are in the closed position, wherein at least a part of the uniform thickness layer is over the predetermined assay sites, and wherein the sample has one or a plurality of analytes that are capable of diffusing in the sample.

In some embodiments, the first plate has, on its surface, at least three analyte assay sites, and the distance between the edges of any two neighboring assay sites is substantially larger than the thickness of the uniform thickness layer when the plates are in the closed position, wherein at least a part of the uniform thickness layer is over the assay sites, and wherein the sample has one or a plurality of analytes that are capable of diffusing in the sample.

In some embodiments, the first plate has, on its surface, at least two neighboring analyte assay sites that are not separated by a distance that is substantially larger than the thickness of the uniform thickness layer when the plates are in the closed position, wherein at least a part of the uniform thickness layer is over the assay sites, and wherein the sample has one or a plurality of analytes that are capable of diffusing in the sample.

In some embodiments, the releasable dry reagent is a cell stain. In some embodiments, the device further comprises a detector that is an optical detector for detecting an optical signal. In some embodiments, the device further comprises a detector that is an electrical detector for detecting an electric signal.

In some embodiments, the device comprises discrete spacers that are not fixed to any of the plates, wherein at the closed configuration, the discrete spacers are between the inner surfaces of the two plates, and the thickness of the sample is confined by the inner surfaces of the two plates, and regulated by the discrete spacers and the plates.

In some embodiments, the device further comprises a binding site that has a chemical sensor that is made from a material selected from the group consisting of: silicon nanowire (Si NW); single-walled carbon nanotubes (SWCNT); random networks of carbon nanotubes (RN-CNTs); molecularly capped metal nanoparticles (MCNPs); metal oxide nanoparticles (MONPs); and chemically sensitive field-effect transistors (CHEM-FETs).

A system is provided herein for rapidly analyzing a vapor condensate sample using a mobile phone comprising:

-   -   (a) a device of any prior claim;     -   (b) a mobile communication device comprising:         -   i. one or a plurality of cameras for the detecting and/or             imaging the vapor condensate sample; and         -   ii. electronics, signal processors, hardware and software             for receiving and/or processing the detected signal and/or             the image of the vapor condensate sample and for remote             communication.

In some embodiments, the system further comprise a light source from either the mobile communication device or an external source.

In some embodiments, one of the plates has a binding site that binds an analyte, wherein at least part of the uniform sample thickness layer is over the binding site, and is substantially less than the average lateral linear dimension of the binding site.

In some embodiments, the system further comprising:

-   -   (d) a housing configured to hold the sample and to be mounted to         the mobile communication device.

In some embodiments, the housing comprises optics for facilitating the imaging and/or signal processing of the sample by the mobile communication device, and a mount configured to hold the optics on the mobile communication device.

In some embodiments, an element of the optics in the housing is movable relative to the housing.

In some embodiments, the mobile communication device is configured to communicate test results to a medical professional, a medical facility or an insurance company.

In some embodiments, the mobile communication device is further configured to communicate information on the test and the subject with the medical professional, medical facility or insurance company.

In some embodiments, the mobile communication device is further configured to communicate information of the test to a cloud network, and the cloud network process the information to refine the test results.

In some embodiments, the mobile communication device is further configured to communicate information of the test and the subject to a cloud network, the cloud network process the information to refine the test results, and the refined test results will send back the subject.

In some embodiments, the mobile communication device is configured to receive a prescription, diagnosis or a recommendation from a medical professional.

Analysis of EBC

Breath tests are among the least invasive methods available for clinical diagnosis, disease state monitoring, health monitoring and environmental exposure assessment. Exemplary methods and devices for analyzing EBC are shown in FIGS. 9-11.

EBC analysis can be used for detection of inflammatory markers, which reflect the state of chronic airways diseases such as chronic obstructive pulmonary disease (COPD), asthma, and cystic fibrosis (CF). EBC analysis can also be used for identification of metabolic, proteomic, and genomic fingerprints of breathing, aiming for an early diagnosis of not only respiratory, but also systemic diseases.

A breath matrix from a subject is a mixture of nitrogen, oxygen, CO2, H2O, and inert gases. The remaining small fraction consists of more than 1000 trace volatile organic compounds (VOCs) with concentrations in the range of parts per million (ppm) to parts per trillion (ppt) by volume. In terms of their origin, these volatile substances may be generated in the body (endogenous) or may be absorbed as contaminants from the environment (exogenous). The composition of VOCs in breath varies widely from person to person, both qualitatively and quantitatively.

Although the number of VOCs found to date in human breath is more than 1000, only a few VOCs are common to all humans. These common VOCs, which include isoprene, acetone, ethane, and methanol, are products of core metabolic processes and are very informative for clinical diagnostics. The bulk matrix and trace VOCs in breath exchange between the blood and alveolar air at the blood-gas interface in the lung. One exception is NO, which is released into the airway in the case of airway inflammation.

The endogenous compounds found in human breath, such as inorganic gases (e.g., NO and CO), VOCs (e.g., isoprene, ethane, pentane, acetone), and other typically nonvolatile substances such as isoprostanes, peroxynitrite, or cytokines, can be measured in breath condensate. Testing for endogenous compounds can provide valuable information concerning a possible disease state. Furthermore, exogenous molecules, particularly halogenated organic compounds, can indicate recent exposure to drugs or environmental pollutants.

Volatile Organic Compounds (VOCs) are organic substances that have a high vapor pressure and therefore evaporate at room temperature. The VOCs that may be assayed as target analytes by the methods and devices provided by the present invention include, but not limited to, biologically generated VOCs (e.g., terpenes, isoprene, methane, green leaf volatiles) and anthropogenic VOCs (e.g., typical solvents used in paints and coatings, like ethyl acetate, glycol ethers, and acetone, vapors from adhesives, paints, adhesive removers, building materials, etc., like methylene chloride, MTBE, and formaldehyde, chlorofurocarbons and perchloroethylene used in dry cleaning, vapor and exhaustive gas from fossil fuels, like benzene and carbon monoxide).

Detailed discussion on certain breath markers for diseases and other health conditions is given in Table 1.

Besides the diseases listed in Table 1, various VOCs contained in exhaled breath have also been linked to different types of cancers. A non-exclusive list of breath VOCs identified as biomarkers for cancers is shown in Table 2.

Besides some of the non-volatile compounds listed in Table 1, various non-volatile compounds have also been lined to or identified as biomarkers of various diseases/conditions. Among these, a particular application of the device and method provided by the present disclosure is to assay the glucose level in EBC. Other applications include, but not limited to, detecting the levels of nitrogen reactive species, arachidonic acid metabolites (e.g., isoprostanes, leukotrienes, prostanoids), cytokines, glutathione, proteins and metabolites, small molecules (e.g., chloride, sodium, potassium, urea, and small organic acids), and pH.

In some embodiments, the devices and methods of the present invention also find applications in the detection of drugs of abuse in EBC sample. The drugs of abuse to be detected using the devices and methods of the present invention include, but not limited to, ethanol, cannabis, methadone, amphetamine, methamphetamine, 3,4-methylenedioxymethamphetamine, codeine, 6-acetylmorphine, diazepam, oxazepam, morphine, benzoylecgonine, cocaine, buprenorphine and tetrahydrocannabinol.

TABLE 1 Breath markers in certain diseases or conditions Disease/Condition Breath Marker Diabetes/diabetic ketoacidosis Acetone, Ethylbenzene, Xylene, Toluene, Ethane, Pentane, Propane, Isoprene, Ethanol, Methanol, Isopropanol, 2,3,4-Trimethylhexane, 2,6,8- Trimethyldecane, Tridecane, Undecane Helicobacter pylori infection Ammonia, volatile organic compounds Uremia/kidney failure Dimethylamine, trimethylamine Liver disease Dimethylamine, trimethylamine Liver disease Ethanethiol, dimethylsulfide, hydrogen disulfide Liver cirrhosis Acetone, styrene, dimethylsulfide, dimethylselene Liver disease/fetor hepaticus C2-C5 Aliphatic acids, methylmercaptan Angina, ischemic heart disease Alkanes, methylated alkanes Heart-transplant rejection Methylated alkane contour Rheumatoid arthritis Pentane Allograft rejection CS2 Oxidative stress NO, CO, nitrosothiol, 8-isoprostane, 4-hydroxy-2- nonenal, malondialdehyde, hydrogen peroxide Chronic obstructive pulmonary NO, CO, nitrosothiol, hydrogen peroxide disease Rhinitis, rhinorrhea chronic cough NO Asthma Pentane, ethane, 8-isoprostane, NO, pH, H2O2, leukotrienes (e.g., LTs, Cys-LTs, LTE4), 8- Isoprostane, PGE2, ILs, IL-4, IL-5, IL-6, IL-8, IL-10, IL-17, INF-□, RANTES, MIP□, MIP□, TNF-□, TGF- □, ET-1, Cytokeratine 1, MDA, ADMA, CCL11, hs- CRP, sICAM-1 Cystic fibrosis NO, CS2, leukotrienes (e.g., LTE4), pH, Nitrotyrosine, Nitrites, Nitric oxide, 8-Isoprostane, IL- 6, IL-8, IL-5, TNF-□ Bronchiectasis NO Lung cancer Alkanes, monomethylated alkanes, nitric oxide Lung carcinoma Acetone, methylethylketone, n-propanol, alkanes, aniline, o-toluidine Breast cancer 2-propanol, 2,3-dihydro-1-4(1H)-quinazolinone, 1- phenyl-ethanone, heptanal, isopropyl myristate Idiopathic pulmonary fibrosis (IPF) 8-Isoprostane, H2O2, 3-nitrotyrosine, NOx, docosatetraenoyl-LPA Pulmonary arterial hypertension Natriuretic peptide, pro-BNP, ET-1, 6-keto-PGF1α, 8- (PAH) isoprostane, IL-6 Sarcoidosis 8-Isoprostane, Cys-LTs, Neopterin, TGF-□ Obstructive SleepApnea Syndrome (OSA) Pediatric patients 8-Isoprostane, IL-6, LTB4, Cys-LTs, H2O2, Uric salts Adult patients 8-Isoprostane, IL-6, TNF-□, pH, H2O2, ICAM-1, IL-8 Systemic Lupus Erythematosus (SLE) IL-6, IL-8, IL-10 Chronic Renal Disease (CRD) pH, Nitrites, Nitrates, H2O2

TABLE 2 VOCs from exhaled breath that are identified in biomarkers of various cancers Disease Compound name Lung cancer 1,3-Cyclopentadiene, 1-methyl- 1-Cyclopentene 2,3-Butanedione 2-Butanol, 2,3-dimethyl- 2-Butanone (methyl ethyl ketone) 2-Butanone, 3-hydroxy- 2-Butene, 2-methyl- 3-Butyn-2-ol Acetophenone Benzaldehyde Benzene, cyclobutyl- Butane, 2-methyl- Butyl acetate Ethylenimine Isoquinoline, 1,2,3,4-tetrahydro- Methyl propyl sulfide n-Pentanal n-Undecane Undecane, 3,7-dimethyl- Urea, tetramethyl- Cyclopentane Acetone Methyl ethyl ketone n-Propanol 1,1′-(1-Butenylidene)bis benzene 1-Methyl-4-(1-methylethyl)benzene 2,3,4-Trimethyl hexane 3,3-Dimethyl pentane Dodecane 1,3-Butadiene, 2-methyl-(isoprene) 1-Heptene 1-Hexene Benzene Benzene, 1,2,4-trimethyl- Benzene, 1,4-dimethyl Benzene, 1-methylethenyl- Benzene, propyl- Cyclohexane Cyclopentane, methyl- Cyclopropane, 1-methyl-2-pentyl- Decane Heptane, 2,2,4,6,6-pentamethyl Heptane, 2,4-dimethyl Heptane, 2-methyl Hexanal Methane, trichlorofluoro- Nonane, 3-methyl- Octane, 3-methyl- Styrene (ethenylbenzene) Undecane Butane Decane, 5-methyl Heptane Hexane, 2-methyl Hexane, 3-methyl Octane, 4-methyl Pentane Tridecane, 3-methyl Tridecane, 7-methyl 1,1-Biphenyl, 2,2-diethyl- 1,2-Benzenedicarboxylic acid, diethyl ester 1,5,9-Cyclododecatriene, 1,5,9-trimethyl- 10,11-Dihydro-5H-dibenz[b,f]azepine 1H-Indene, 2,3-dihydro-1,1,3-trimethyl-3-phenyl- 1-Propanol 2,4-Hexadiene, 2,5-dimethyl- 3-Pentanone, 2,4-dimethyl- 2,5-Cyclohexadiene-1,4-dione, 2,6-bis(1,1-dimethylethyl)- Benzene, 1,1-oxybis- Benzoic acid, 4-ethoxy-, ethyl ester Decane, 4-methyl- Furan, 2,5-dimethyl- Pentan-1,3-dioldiisobutyrate, 2,2,4-trimethyl Propanoic acid, 2-methyl-, 1-(1,1-dimethylethyl)-2-methyl-1,3- propanediyl ester trans-Caryophyllene 1,2,4,5-Tetroxane, 3,3,6,6-tetraphenyl- 1H-Indene, 2,3-dihydro-4-methyl- 1-Propene, 1-(methylthio)-, (E)- 2,2,4-Trimethyl-1,3-pentanediol diisobutyrate 2,2,7,7-Tetramethyltricyclo-[6.2.1.0(1,6)]undec-4-en-3-one 2,3-Hexanedione 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-ethylidene 2-Methyl-3-hexanone 4-Penten-2-ol 5,5-Dimethyl-1,3-hexadiene 5-Isopropenyl-2-methyl-7-oxabicyclo[4.1.0]heptan-2-ol 9,10-Anthracenediol, 2-ethyl- Anthracene, 1,2,3,4-tetrahydro-9-propyl- Benzene, 1,1-(1,2-cyclobutanediyl)bis,cis- Benzene, 1,1-[1-(ethylthio)propylidene]bis- Benzene, 1,1-ethylidenebis, 4-ethyl- Benzophenone Bicyclo[3.2.2]nonane-1,5-dicarboxylic acid, 5-ethyl ester Camphor Ethane, 1,1,2-trichloro-1,2,2-trifluoro- Furan, 2-[(2-ethoxy-3,4-dimethyl-2-cyclohexen-1-ylidene)methyl]- Isomethyl ionone Isopropyl alcohol Pentanoic acid, 2,2,4-trimethyl-3-carboxyisopropyl, isobutyl ester Propane, 2-methoxy-2-methyl- α-Isomethyl ionone Butanal Heptanal Nonanal Octanal Pentanal Propanal Ethylbenzene Octane Pentamethylheptane Toluene 2-Methylpentane Isoprene Xylenes total Styrene Aniline o-Toluidine 1-Butanol 3-Hydroxy-2-butanone 2,6,10-T rimethyltetradecane 2,6,11-Trimethyldodecane 2,6-Dimethylnaphthalene 2,6-Di-tert-butyl-, 4-methylphenol 2-Methylhendecanal 2-Methylnaphthalene 2-Pentadecanone 3,7-Dimethylpentadecane 3,8-Dimethylhendecane 4-Methyltetradecane 5-(1-Methyl)propylnonane 5-(2-Methyl)propylnonane 5-Butylnonane 5-Propyltridecane 7-Methylhexadecane 8-Hexylpentadecane 8-Methylheptadecane Eicosane Hexadecanal Nonadecane Nonadecanol Tridecane Tridecanone Formaldehyde (methanal) Isopropanol Breast cancer 2,3,4-Trimethyldecane 2-Amino-5-isopropyl-8-methyl-1-azulenecarbonitrile 3,3-Dimethyl pentane 5-(2-Methylpropyl)nonane 6-Ethyl-3-octyl ester 2-trifluoromethyl benzoic acid Nonane Tridecane, 5-methyl Undecane, 3-methyl Pentadecane, 6-methyl Propane, 2-methyl Nonadecane, 3-methyl Dodecane, 4-methyl Octane, 2-methyl 1-Phenylethanone 2,3-Dihydro-1-phenyl-4(1H)-quinazolinone 2-Propanol Heptanal Isopropyl myristate (+)-Longifolene 1,3-Butadiene, 2-methyl- 1,4-Pentadiene 1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene- 1-Octanol, 2-butyl- 2,5-Cyclohexadiene-1,4-dione, 2,6-bis(1,1-dimethylethyl)- 2,5-Di-tert-butyl-1,4-benzoquinone 2-Hexyl-1-octanol 3-Ethoxy-1,1,1,5,5,5-hexamethyl-3-(trimethylsiloxy)trisiloxane Acetic acid, 2,6,6-trimethyl-3-methylene-7-(3-oxobutylidene)oxepan-2-yl ester Benzene, 1,2,3,5-tetramethyl- Benzene, 1,2,4,5-tetramethyl- Benzene, 1-ethyl-3,5-dimethyl- Benzoic acid, 4-methyl-2-trimethylsilyloxy-, trimethylsilyl ester Cyclohexene, 1-methyl-5-(1-methylethenyl)- Cyclohexene, 1-methyl-5-(1-methylethenyl)-, (R)- Cyclopropane, ethylidene Cyclotetrasiloxane, octamethyl- D-Limonene Dodecane Dodecane, 2,6,11-trimethyl- Dodecane, 2,7,10-trimethyl- Longifolene-(V4) Pentadecane Tetradecane Tridecane Trifluoroacetic acid, n-octadecyl ester Undecane Colon cancer 1,1′-(1-Butenylidene)bis benzene 1,3-Dimethylbenzene 4-(4-Propylcyclohexyl)-4′-cyano[1,1′-biphenyl]-4-yl ester benzoic acid 2-Amino-5-isopropyl-8-methyl-1-azulenecarbonitrile [(1,1-Dimethylethyl)thio]acetic acid Esophagogastric Ethylphenol cancer Hexanoic acid Methylphenol Phenol Gastric cancer 2-Butoxyethanol Isoprene 2-Propenenitrile 6-Methyl-5-hepten-2-one Furfural (furfuraldehyde) Head and neck 4,6-Dimethyldodecane cancer 5-Methyl-3-hexanone 2,2-Dimethyldecane Limonene 2,2,3-Trimethyl-exobicyclo[2.2.1]heptane 2,2-Dimethyl-propanoic acid Ammonium acetate 3-Methylhexane 2,4-Dimethylheptane 4-Methyloctane p-Xylene 2,6,6-Trimethyloctane 3-Methylnonane Liver cancer 3-Hydroxy-2-butanone Styrene Decane Ovarian cancer Decanal Nonanal Styrene 2-Butanone Hexadecane Prostate cancer Toluene p-Xylene 2-Amino-5-isopropyl-8-methyl-1-azulenecarbonitrile 2,2-Dimethyldecane EBC-3.2. Collection and Analysis of Other Vapor Condensates.

Certain embodiments of the present invention are related to the applications of the SiEBCA methods and devices for collection and analysis of the vapor condensates other than the EBC. The other moistures include, but not limited to, fog, clouds, steams, etc. The target analysis of these vapor condensates can be for different purpose environmental monitoring, emission control, etc. In some embodiments, the sample is a vapor from a biological sample, an environmental sample, a chemical sample, or clinical sample.

EBC-3.3. Automatic and High Throughput.

In certain embodiments, the devices and methods of the present invention are automatic and high speed, where the steps are performed by machines. In some embodiments, the plates are in the form of roll of sheets and are controlled by rollers to put certain area of the plates into an open configuration or a closed configuration.

EBC-3.4. Identification and Validation of Markers in Vapor Condensate

In certain embodiments, the devices and methods of the present invention are particularly useful for the identification and validation of biomarkers for human diseases/conditions, or other markers for environmental, food safety, or other conditions/events. Due to the ease, fast speed, small sample volume, and multiplexing potential of the present devices and methods, it is easy to adapt the present device for high-throughput and even automatic screening and validation of these markers. In certain embodiments, the present devices and methods are particularly useful when coupled with data processing system capable of pattern recognition for such purposes.

In certain embodiments, the devices and methods of the present invention are also advantageous to create large sample dataset for refining the algorithms for pattern recognition through machine learning and/or other methodologies.

EBC-4. EBC Collection and Analysis without Spacers

Another aspect of the present invention is to provide devices and methods for collecting and analyzing vapor condensate using the aforementioned collection plate and cover plate but without spacers.

In some embodiments of the present invention, the spacers that are used to regulate the sample or a relevant volume of the EBC sample are replaced by (a) positioning sensors that can measure the plate inner spacing, and/or (b) devices that can control the plate positions and move the plates into a desired plate inner spacing based on the information provided the sensors. In some embodiment, all the spacers are replaced by translation stage, monitoring sensors and feedback system.

In some embodiments, the collection plate and the cover plate comprise no spacers at all, and the EBC sample is compressed by the two plates into a thin layer, the thickness of which is regulated by the spacing between the inner surfaces of the plates (the plate spacing).

-   A4. A device for collecting EBC without spacers, comprises:

a first plate and a second plate, wherein:

-   -   i. the plates are movable relative to each other into different         configurations, and one or both plates are flexible;     -   ii. both plates comprise a sample contact area on the respective         surface of each plate for contacting EBC sample;         -   wherein one of the configurations is an open configuration,             in which: the two plates are separated apart, and the EBC             sample is deposited on one or both of the plates from a             subject; and         -   wherein another of the configurations is a closed             configuration which is configured after the EBC sample             deposition in the open configuration; and in the closed             configuration: at least part of the EBC sample is compressed             by the two plates into a thin layer, wherein the thin layer             is in contact with and confined by the inner surfaces of the             two plates.

-   A5. A method of collecting EBC without spacers, comprises the steps:     -   (a) obtaining a collection plate and a cover plate of paragraph         A4;     -   (b) depositing, when the plates are configured in the open         configuration, an EBC sample by exhaling breath from a subject         toward the collection plate, wherein the exhaled breath         condensates on a collection surface of the collection plate to         form droplets and/or puddles that have different lateral sizes         and different heights, depending upon the surface wetting         properties of the collection surface;     -   (c) after (b), bringing the cover plate over the collection         surface and then bringing the two plates into a closed         configuration by pressing the plates, wherein at the closed         configuration:         -   (i) at least a part of the EBC sample is between the cover             plate and the collection plate, and a relevant area of the             collection surface of the collection plate is covered by the             cove plate; and         -   (ii) in the relevant area, a substantial number or all of             the droplets or puddles formed in step (b) at the open             configuration merge into puddle(s) that (1) have much larger             lateral size but in a smaller number than the open             configuration and (2) touch both inner surfaces of the cover             plate and the collection plate, thereby the thickness of the             puddle(s) is confined by the inner surfaces of the plates             and equal to the spacing between the inner surfaces, and the             total surface area of the deposited EBC exposed to the             ambient is significantly reduced; and

wherein the plate spacing is the spacing between the inner surfaces of the cover plate and the collection plate, the relevant area is a portion or entire surface of the collection surface, and the collection surface is a portion or entire surface of the collection plate.

-   A6. A method of analyzing EBC without spacers, comprises the steps:     -   (a) obtaining a collection plate and a cover plate of paragraph         A4;     -   (b) depositing, when the plates are configured in the open         configuration, an EBC sample by exhaling breath from a subject         toward the collection plate, wherein the exhaled breath         condensates on a collection surface of the collection plate to         form droplets and/or puddles that have different lateral sizes         and different heights, depending upon the surface wetting         properties of the collection surface;     -   (c) after (b), bringing the cover plate over the collection         surface and then bringing the two plates into a closed         configuration by pressing the plates, wherein at the closed         configuration:         -   (i) at least a part of the EBC sample is between the cover             plate and the collection plate, and a relevant area of the             collection surface of the collection plate is covered by the             cove plate; and         -   (ii) in the relevant area, a substantial number or all of             the droplets or puddles formed in step (b) at the open             configuration merge into puddle(s) that (1) have much larger             lateral size but in a smaller number than the open             configuration and (2) touch both inner surfaces of the cover             plate and the collection plate, thereby the thickness of the             puddle(s) is confined by the inner surfaces of the plates             and equal to the spacing between the inner surfaces, and the             total surface area of the deposited EBC exposed to the             ambient is significantly reduced; and     -   (d) analyzing the EBC,

wherein the plate spacing is the spacing between the inner surfaces of the cover plate and the collection plate, the relevant area is a portion or entire surface of the collection surface, and the collection surface is a portion or entire surface of the collection plate.

In some embodiments, it is unlikely to obtain a layer of highly uniform thickness without using the spacers as discussed in the foregoing sessions. However, it is still advantageous to use the device and method of paragraphs A4-A5 for collecting and analyzing EBC sample, for it is easy, rapid to handle, requires no professional training and a very small volume of sample.

In some embodiments, the analyzing step (d) of paragraph A6 comprises determining the thickness of the collected EBC sample at the closed configuration after the formation of the thin layer during step (c). In some embodiments, the thickness of the collected EBC sample at the closed configuration is equal to the spacing between the inner surfaces of the two plates.

In some embodiments, measuring the spacing between the inner surfaces comprises the use of optical interference. The optical interference can use multiple wavelength. For example, the light signal due to the interference of a light reflected at the inner surface of the first plate and the second plate oscillate with the wavelength of the light. From the oscillation, one can determine the spacing between the inner surfaces. To enhance the interference signal, one of the inner surfaces or both can be coated with light reflection material.

In some embodiments, measuring the spacing between the inner surfaces comprises taking optical imaging (e.g. taking a 2D (two-dimensional)/3D (three-dimensional) image of the sample and the image taking can be multiple times with different viewing angles, different wavelength, different phase, and/or different polarization) and image processing.

In some embodiments, the analyzing step (d) of paragraph A6 comprises measuring the volume of the collected EBC sample based on the lateral area and the thickness of the thin layer that are determined after the formation of the thin layer during step (c).

In some embodiments, measuring the entire sample area or volume comprises taking optical imaging (e.g. taking a 2D (two-dimensional)/3D (three-dimensional) image of the sample and the image taking can be multiple times with different viewing angles, different wavelength, different phase, and/or different polarization) and image processing. The sample lateral area means the area in the direction approximately parallel to the first plate and the second plate. The 3D imaging can use the method of fringe projection profilometry (FPP), which is one of the most prevalent methods for acquiring three-dimensional (3D) images of objects.

In some embodiments, the measuring of the sample area or volume by imaging comprises: (a) calibration of the image scale by using a sample of the known area or volume (e.g., The imager is a smartphone and the dimensions of the image taken by the phone can be calibrated by comparing an image of the a sample of known dimension taken the same phone); (b) comparison of the image with the scale markers (rulers) placed on or near the first plate and second plate (discussed further herein), and (c) a combination of thereof.

As used herein, light may include visible light, ultraviolet light, infrared light, and/or near infrared light. Light may include wavelengths in the range from 20 nm to 20,000 nm.

In some embodiments, the pressing during step (c) of paragraphs A5-A6 is performed by human hand.

In some embodiments, the formation and properties of the thin layer is dependent on the pressing force applied during step (c) of paragraphs A5-A6 for bringing the two plates into the closed configuration. In some embodiments, the pressing force applied during step (c) of paragraphs A5-A6 is well adjusted for forming a thin layer of EBC sample between the two plates that has prerequisite parameters.

More Examples of EBC Collection and Analysis Experiments

Additional exemplary experimental testing and observation, and additional preferred embodiments of the present invention are given.

All the exemplary experimental testing and demonstration of the present invention described in Section 4 (Examples) were performed under the following conditions and share the following common observations.

Plates.

Only one of the two plates of SiEBCA device, termed “X-Plate”, has the spacers fixed on the sample surface of the plate, and the other plate, termed “the substrate plate”, has a planar surface and does not have spacers.

EBC Formation with No Spacers at Open and Closed Configurations

In a separate set of experiments, we tested the possibility of collecting EBC samples using plates with no spacers.

As presented here, the exemplary SiEBCA device also comprises a collection plate and a cover plate, while the collection plate we used was 25 mm×25 mm×1 mm PMMA planar plate with untreated surfaces, and the cover plate was 25 mm×25 mm×0.175 mm PMMA planar plate with bare untreated surfaces. The EBC sample was collected by having a subject breathe on a collection plate for 2 sec and a cover plate was immediately brought to cover the collection plate and pressed against it as described above. Later, the SiEBCA together with the sample collected therein were subject to optical measurement and microscopy imaging.

FIG. 15 in U.S. Provisional Patent Application 62/459,972, filed on Feb. 16, 2017, which is herein incorporated by reference in its entirety, schematically illustrates the optical measurement and imaging taken for the measurement of the EBC sample thickness and lateral area, respectively. As shown in panel (A), Fabry-Pérot interferometer was used to measure the F-P cavity resonance in the reflectance spectra at 25 points on the 4×4 grid artificially generated in the center of the SiEBCA device, from which the plate spacing (and the sample thickness) is thus deduced. Each of the 25 measuring points is about 2 um by 2 um in area, and all 25 points cover an area of 20 mm by 20 mm. An average plate spacing over the 25 points was taken as the estimate of the sample thickness (

). As shown in panel (B), a direct photo of the SiEBCA device was taken to delineate the general contour of the EBC sample between the two plates and measure the overall lateral area (S_(t)). Then microscopic images were taken at each of the 25 points (each image covers an area S_(i) of 1.6 mm×1.1 mm), and then these images were analyzed by an image processing software to recognize and measure the total area of the air bubbles (S_(b)) in each image.

To estimate the total EBC sample lateral area, first, the percentage of EBC liquid lateral area (a_(i)) for each measuring point is calculated as (Si−Sb)/Si×100%; second, an average value (ã) is taken from all 25 points; and finally, the total EBC sample lateral area (S_(EBC)) is estimated as S_(t)*ã.

The volume of the EBC sample (V_(EBC)) is thus determined as S_(EBC)

FIG. 16 in U.S. Provisional Patent Application 62/459,972, filed on Feb. 16, 2017, which is herein incorporated by reference in its entirety, demonstrates the principle of plate spacing measurement based on F-P cavity resonance. Panel (a) shows the schematic of F-P cavity from the SiEBCA device; panel (b) shows the typical reflectance spectrum and resonances from the device. The plate spacing (h) at each measuring point is calculated as:

$h = \frac{c}{2n\Delta v}$

where h is the plate spacing, c is light speed, Δv is the period in frequency domain and n is the reflective index of the EBC liquid.

As described above, the average EBC sample thickness is equal to

$\frac{\Sigma_{1}^{25}h}{25}.$

EBC sample thickness uniformity is calculated as

$\sqrt{\frac{{\Sigma_{1}^{25}\left( {h - H} \right)}^{2}}{25}}.$

FIG. 17 in U.S. Provisional Patent Application 62/459,972, filed on Feb. 16, 2017, which is herein incorporated by reference in its entirety, shows microscopic images of the EBC sample collected using the exemplary SiEBCA device without spacers. Panels (a)-(b) respectively show the images of the EBC samples at the closed configuration after hand pressing the two plates with low, medium, and high pressing strength. Low strength was less than 10 kg, high strength was higher than 15 kg, and medium strength was in between the low and high strength.

Under these three different conditions, the performance of the exemplary SiEBCA device without spacers was examined and summarized in Table 3, based on the measurement and calculation methods described above. As shown in Table 3 and FIG. 17, low strength gives thicker liquid thickness with larger bubble area, while high strength gives thinner EBC sample layer with smaller bubble area.

TABLE 3 Performance of SiEBCA without spacers Average EBC Average Collected EBC Area EBC EBC EBC Press area S_(EBC) thickness volume thickness Strength percentage ã (mm²)

  V_(EBC) (uL) uniformity 1 Low 38% 240 1.45 0.35 58% 2 Medium 72% 450 0.87 0.39 47% 3 High 98% 620 0.51 0.32 43%

-   AA0. A device for collecting and analyzing vapor condensate (VC)     sample, comprising:

a collection plate and a cover plate, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible; and     -   iii. each of the plates has, on its inner respective surface, a         sample contact area for contacting a vapor condensate (VC)         sample that contains an analyte;         -   wherein one of the configurations is an open configuration,             in which: the two plates are either completely or partially             separated apart, and the VC sample is deposited on one or             both of the plates; and         -   wherein another of the configurations is a closed             configuration which is configured after the VC sample             deposition in the open configuration; and in the closed             configuration: at least a part of the VC sample is between             the two plates and in contact with the two plates, and has a             thickness that is regulated by the two sample surfaces of             the plates and is equal to or less than 30 □m with a small             variation.

-   AA1. A device for collecting and analyzing vapor condensate (VC)     sample, comprising:

a collection plate, a cover plate, and spacers, wherein:

-   -   i. the plates are movable relative to each other into different         configurations;     -   ii. one or both plates are flexible;     -   iii. each of the plates has, on its respective inner surface, a         sample contact area for contacting a vapor condensate (VC)         sample that contains an analyte;     -   iv. the spacers are fixed to the respective inner surface of one         or both of the plates and have a predetermined substantially         uniform height and a predetermined constant inter-spacer         distance and wherein at least one of the spacers is inside the         sample contact area;     -   wherein one of the configurations is an open configuration, in         which: the two plates are either completely or partially         separated apart, the spacing between the plates is not regulated         by the spacers, and the VC sample is deposited on one or both of         the plates; and     -   wherein another of the configurations is a closed configuration         which is configured after the VC sample deposition in the open         configuration; and in the closed configuration: at least a part         of the VC sample is between the two plates and in contact with         the two plates, and has a highly uniform thickness that is         regulated by the spacers and the two sample surfaces of the         plates and is equal to or less than 30 □m with a small         variation.

-   AA2. The device of embodiment AA0 or AA1, wherein the device further     comprises a dry reagent coated on one or both of the plates.

-   AA3. The device of any prior embodiment, wherein the device further     comprises, on one or both plates, a dry binding site that has a     predetermined area, wherein the dry binding site binds to and     immobilizes an analyte in the sample.

-   AA4. The device of any prior embodiment, wherein the device further     comprises, on one or both plates, a releasable dry reagent and a     release time control material that delays the time that the     releasable dry regent is released into the sample.

-   AA5. The device of embodiment 4, wherein the release time control     material delays the time that the dry regent starts is released into     the sample by at least 3 seconds.

-   AA6. The device of any prior embodiment, wherein the device further     comprises, on one or both plates, one or a plurality of dry binding     sites and/or one or a plurality of reagent sites.

-   AA7. The device of any prior embodiment, wherein the sample is     exhale breath condensate.

-   AA8. The device of any prior embodiment, wherein the sample is a     vapor from a biological sample, an environmental sample, a chemical     sample, or clinical sample.

-   AA9. The device of any prior embodiment, wherein the analyte     comprises a molecule (e.g., a protein, peptides, DNA, RNA, nucleic     acid, or other molecules), cells, tissues, viruses, and     nanoparticles with different shapes.

-   AA10. The device of any prior embodiment, wherein the analyte     comprises volatile organic compounds (VOCs).

-   AA11. The device of any prior embodiment, wherein the analyte     comprises nitrogen, oxygen, CO2, H2O, and inert gases.

-   AA12. The device of any prior embodiment, wherein the analyte is     stained.

-   AA13. The device of any prior embodiment, wherein on one of the     sample surface, it further comprises an enclosure-spacer that     encloses a partial or entire VC samples deposited on the collection     plate.

-   AA14. The device of any prior embodiment, wherein the highly uniform     thickness has a value equal to or less than 0.5 um.

-   AA15. The device of any prior embodiment, wherein the highly uniform     thickness has a value in the range of 0.5 um to 1 um.

-   AA16. The device of any prior embodiment, wherein the highly uniform     thickness has a value in the range of 1 um to 2 um.

-   AA17. The device of any prior embodiment, wherein the highly uniform     thickness has a value in the range of 2 um to 10 um.

-   AA18. The device of any prior embodiment, wherein the highly uniform     thickness has a value in the range of 10 um to 20 um.

-   AA19. The device of any prior embodiment, wherein the highly uniform     thickness has a value in the range of 20 um to 30 um.

-   AA20. The device of any prior embodiment, wherein the thickness of     the at least a part of VC sample at the closed configuration is     larger than the thickness of VC sample deposited on the collection     plate at an open configuration.

-   AA21. The device of any prior embodiment, wherein the thickness of     the at least a part of VC sample at the closed configuration is less     than the thickness of VC sample deposited on the collection plate at     an open configuration.

-   AA22. The device of any prior device embodiment, wherein the spacers     are fixed on a plate by directly embossing the plate or injection     molding of the plate.

-   AA23. The device of any prior device embodiment, wherein the     materials of the plate and the spacers are selected from     polystyrene, PMMA, PC, COC, COP, or another plastic.

-   AA24. The device of any prior embodiment, wherein the inter-spacer     spacing is in the range of 1 um to 200 um.

-   AA25. The device of any prior embodiment, wherein the inter-spacer     spacing is in the range of 200 um to 1000 um.

-   AA26. The device of any prior embodiment, wherein the VC sample is     an exhaled breath condensate from a human or an animal.

-   AA27. The device of any prior embodiment, wherein the spacers     regulating the layer of uniform thickness have a filling factor of     at least 1%, wherein the filling factor is the ratio of the spacer     area in contact with the layer of uniform thickness to the total     plate area in contact with the layer of uniform thickness.

-   AA28. The device of any prior embodiment, wherein for spacers     regulating the layer of uniform thickness, the Young's modulus of     the spacers times the filling factor of the spacers is equal to or     larger than 10 MPa, wherein the filling factor is the ratio of the     spacer area in contact with the layer of uniform thickness to the     total plate area in contact with the layer of uniform thickness.

-   AA29. The device of any prior embodiment, wherein for a flexible     plate, the thickness of the flexible plate times the Young's modulus     of the flexible plate is in the range 60 to 750 GPa-um.

-   AA30. The device of any prior embodiment, wherein for a flexible     plate, the fourth power of the inter-spacer-distance (ISD) divided     by the thickness of the flexible plate (h) and the Young's     modulus (E) of the flexible plate, ISD4/(hE), is equal to or less     than 106 um3/GPa,

-   AA31. The device of any prior paragraph, wherein one or both plates     comprises a location marker, either on a surface of or inside the     plate, that provides information of a location of the plate.

-   AA32. The device of any prior paragraph, wherein one or both plates     comprises a scale marker, either on a surface of or inside the     plate, that provides information of a lateral dimension of a     structure of the sample and/or the plate.

-   AA33. The device of any prior embodiment, wherein one or both plates     comprises an imaging marker, either on surface of or inside the     plate, that assists an imaging of the sample.

-   AA34. The device of any prior embodiment, wherein the spacers     function as a location marker, a scale marker, an imaging marker, or     any combination of thereof.

-   AA35. The device of any prior embodiment, wherein the average     thickness of the layer of uniform thickness is about equal to a     minimum dimension of an analyte in the sample.

-   AA36. The device of any prior embodiment, wherein the inter-spacer     distance is in the range of 1 □m to 50 □m.

-   AA37. The device of any prior embodiment, wherein the inter-spacer     distance is in the range of 50 □m to 120 □m.

-   AA38. The device of any prior embodiment, wherein the inter-spacer     distance is in the range of 120 □m to 200 □m.

-   AA39. The device of any prior embodiment, wherein the inter-spacer     distance is substantially periodic.

-   AA40. The device of any prior embodiment, wherein the inter-spacer     distance is aperiodic.

-   AA41. The device of any prior embodiment, wherein the spacers are     pillars with a cross-sectional shape selected from round, polygonal,     circular, square, rectangular, oval, elliptical, or any combination     of the same.

-   AA42. The device of any prior embodiment, wherein the spacers have a     pillar shape and have a substantially flat top surface, wherein, for     each spacer, the ratio of the lateral dimension of the spacer to its     height is at least 1.

-   AA43. The device of any prior embodiment, wherein each spacer has a     ratio of the lateral dimension of the spacer to its height at least     1.

-   AA44. The device of any prior embodiment, wherein the minimum     lateral dimension of spacer is less than or substantially equal to     the minimum dimension of an analyte in the sample.

-   AA45. The device of any prior embodiment, wherein the minimum     lateral dimension of spacer is in the range of 0.5 um to 100 um.

-   AA46. The device of any prior embodiment, wherein the minimum     lateral dimension of spacer is in the range of 0.5 um to 10 um.

-   AA47. The device of any prior embodiment, wherein the spacers have a     density of at least 100/mm².

-   AA48. The device of any prior embodiment, wherein the spacers have a     density of at least 1000/mm².

-   AA49. The device of any prior embodiment, wherein at least one of     the plates is transparent.

-   AA50. The device of any prior embodiment, wherein at least one of     the plates is made from a flexible polymer.

-   AA51. The device of any prior embodiment, wherein, for a pressure     that compresses the plates, the spacers are not compressible and/or,     independently, only one of the plates is flexible.

-   AA52. The device of any of any prior embodiment, wherein the     flexible plate has a thickness in the range of 10 □m to 200 □m.

-   AA53. The device of any prior embodiment, wherein the variation is     less than 30%.

-   AA54. The device of any prior embodiment, wherein the variation is     less than 10%.

-   AA55. The device of any prior embodiment, wherein the variation is     less than 5%.

-   AA56. The device of any prior embodiment, wherein the first and     second plates are connected and are configured to be changed from     the open configuration to the closed configuration by folding the     plates.

-   AA57. The device of any prior embodiment, wherein the first and     second plates are connected by a hinge and are configured to be     changed from the open configuration to the closed configuration by     folding the plates along the hinge.

-   AA58. The device of any prior embodiment, wherein the first and     second plates are connected by a hinge that is a separate material     to the plates, and are configured to be changed from the open     configuration to the closed configuration by folding the plates     along the hinge.

-   AA59. The device of any prior embodiment, wherein the first and     second plates are made in a single piece of material and are     configured to be changed from the open configuration to the closed     configuration by folding the plates.

-   AA60. The device of any prior embodiment, wherein the layer of     uniform thickness sample is uniform over a lateral area that is at     least 100 um².

-   AA61. The device of any prior embodiment, wherein the layer of     uniform thickness sample is uniform over a lateral area that is at     least 1 mm².

-   AA62. The device of any prior embodiment, wherein the device is     configured to analyze the sample in 60 seconds or less.

-   AA63. The device of any prior embodiment, wherein at the closed     configuration, the final sample thickness device is configured to     analyze the sample in 60 seconds or less.

-   AA64. The device of any prior embodiment, wherein the device further     comprises, on one or both of the plates, one or a plurality of     amplification sites that are each capable of amplifying a signal     from the analyte or a label of the analyte when the analyte or label     is within 500 nm from an amplification site.

-   AA65. The device of any prior embodiment, wherein at the closed     configuration, the final sample thickness device is configured to     analyze the sample in 10 seconds or less.

-   AA66. The device of any prior embodiment, wherein the dry binding     site comprises a capture agent.

-   AA67. The device of any prior embodiment, wherein the dry binding     site comprises an antibody or nucleic acid.

-   AA68. The device of any prior embodiment, wherein the releasable dry     reagent is a labeled reagent.

-   AA69. The device of any prior embodiment, wherein the releasable dry     reagent is a fluorescently-labeled reagent.

-   AA70. The device of any prior embodiment, wherein the releasable dry     reagent is a fluorescently-labeled antibody.

-   AA71. The device of any prior embodiment, wherein the first plate     further comprises, on its surface, a first predetermined assay site     and a second predetermined assay site, wherein the distance between     the edges of the assay site is substantially larger than the     thickness of the uniform thickness layer when the plates are in the     closed position, wherein at least a part of the uniform thickness     layer is over the predetermined assay sites, and wherein the sample     has one or a plurality of analytes that are capable of diffusing in     the sample.

-   AA72. The device of any prior embodiment, wherein the first plate     has, on its surface, at least three analyte assay sites, and the     distance between the edges of any two neighboring assay sites is     substantially larger than the thickness of the uniform thickness     layer when the plates are in the closed position, wherein at least a     part of the uniform thickness layer is over the assay sites, and     wherein the sample has one or a plurality of analytes that are     capable of diffusing in the sample.

-   AA73. The device of any prior embodiment, wherein the first plate     has, on its surface, at least two neighboring analyte assay sites     that are not separated by a distance that is substantially larger     than the thickness of the uniform thickness layer when the plates     are in the closed position, wherein at least a part of the uniform     thickness layer is over the assay sites, and wherein the sample has     one or a plurality of analytes that are capable of diffusing in the     sample.

-   AA74. The device of any prior embodiment, wherein the releasable dry     reagent is a cell stain.

-   AA75. The device of any prior embodiment, wherein the device further     comprises a detector that is an optical detector for detecting an     optical signal.

-   AA76. The device of any prior embodiment, wherein the device further     comprises a detector that is an electrical detector for detecting an     electric signal.

-   AA77. The device of any prior embodiment, wherein the device     comprises discrete spacers that are not fixed to any of the plates,     wherein at the closed configuration, the discrete spacers are     between the inner surfaces of the two plates, and the thickness of     the sample is confined by the inner surfaces of the two plates, and     regulated by the discrete spacers and the plates.

-   AA78. The device of any prior embodiment, wherein the device further     comprises a binding site that has a chemical sensor that is made     from a material selected from the group consisting of: silicon     nanowire (Si NW; single-walled carbon nanotubes (SWCNT); random     networks of carbon nanotubes (RN-CNTs); molecularly capped metal     nanoparticles (MCNPs); metal oxide nanoparticles (MONPs); and     chemically sensitive field-effect transistors (CHEM-FETs).

-   BB1. A system for rapidly analyzing a vapor condensation sample     using a mobile phone comprising:     (a) a device of any prior AA embodiment;     (b) a mobile communication device comprising:     i. one or a plurality of cameras for the detecting and/or imaging     the vapor condensate sample; and     ii. electronics, signal processors, hardware and software for     receiving and/or processing the detected signal and/or the image of     the vapor condensate sample and for remote communication.

-   BB2. The system of any prior BB embodiment, wherein the system     further comprise a light source from either the mobile communication     device or an external source.

-   BB3. The system of any prior BB embodiment, wherein one of the     plates has a binding site that binds an analyte, wherein at least     part of the uniform sample thickness layer is over the binding site,     and is substantially less than the average lateral linear dimension     of the binding site.

-   BB4. The system of any prior BB embodiment, further comprising:     (d) a housing configured to hold the sample and to be mounted to the     mobile communication device.

-   BB5. The system of any prior BB embodiment, wherein the housing     comprises optics for facilitating the imaging and/or signal     processing of the sample by the mobile communication device, and a     mount configured to hold the optics on the mobile communication     device.

-   BB6. The system of any prior BB embodiment, wherein an element of     the optics in the housing is movable relative to the housing.

-   BB7. The system of any prior BB embodiment, wherein the mobile     communication device is configured to communicate test results to a     medical professional, a medical facility or an insurance company.

-   BB8. The system of any prior BB embodiment, wherein the mobile     communication device is further configured to communicate     information on the test and the subject with the medical     professional, medical facility or insurance company.

-   BB9. The system of any prior BB embodiment, wherein the mobile     communication device is further configured to communicate     information of the test to a cloud network, and the cloud network     process the information to refine the test results.

-   BB10. The system of any prior BB embodiment, wherein the mobile     communication device is further configured to communicate     information of the test and the subject to a cloud network, the     cloud network process the information to refine the test results,     and the refined test results will send back the subject.

-   BB11. The system of any prior BB embodiment, wherein the mobile     communication device is configured to receive a prescription,     diagnosis or a recommendation from a medical professional.

-   BB12. The system of any prior BB embodiment, wherein the mobile     communication device is configured with hardware and software to:     (a) capture an image of the sample;     (b) analyze a test location and a control location in in image; and     (c) compare a value obtained from analysis of the test location to a     threshold value that characterizes the rapid diagnostic test.

-   BB13. The system of any prior BB embodiment, wherein at least one of     the plates comprises a storage site in which assay reagents are     stored.

-   BB14. The system of any prior BB embodiment, at least one of the     cameras reads a signal from the CROF device.

-   BB15. The system of any prior BB embodiment, wherein the mobile     communication device communicates with the remote location via a     wifi or cellular network.

-   BB16. The system of any prior BB embodiment, wherein the mobile     communication device is a mobile phone.

-   CC1. A method for rapidly analyzing an analyte in a sample using a     mobile phone, comprising:     (a) depositing a sample on the device of any prior BB embodiment;     (b) assaying an analyte in the sample deposited on the device to     generate a result; and     (c) communicating the result from the mobile communication device to     a location remote from the mobile communication device.

-   CC2. The method of any prior CC embodiment, wherein the analyte     comprises a molecule (e.g., a protein, peptides, DNA, RNA, nucleic     acid, or other molecule), cells, tissues, viruses, and nanoparticles     with different shapes.

-   CC3. The method of any prior CC embodiment, wherein the analyte     comprises white blood cell, red blood cell and platelets.

-   CC4. The method of any prior CC embodiment, wherein the method     comprises:     analyzing the results at the remote location to provide an analyzed     result; and communicating the analyzed result from the remote     location to the mobile communication device.

-   CC5. The method of any prior CC embodiment, wherein the analysis is     done by a medical professional at a remote location.

-   CC6. The method of any prior CC embodiment, wherein the mobile     communication device receives a prescription, diagnosis or a     recommendation from a medical professional at a remote location.

-   CC7. The method of any prior CC embodiment, wherein the thickness of     the at least a part of VC sample at the closed configuration is     larger than the thickness of VC sample deposited on the collection     plate at an open configuration.

-   CC8. The method of any prior CC embodiment, wherein the thickness of     the at least a part of VC sample at the closed configuration is less     than the thickness of VC sample deposited on the collection plate at     an open configuration.

-   CC9. The method of any prior CC paragraph, wherein the assaying step     comprises detecting an analyte in the sample.

-   CC10. The method of any prior CC paragraph, wherein the analyte is a     biomarker.

-   CC11. The method of any prior CC embodiment, wherein the analyte is     a protein, nucleic acid, cell, or metabolite.

-   CC12. The method of any prior CC embodiment, wherein the assay done     in step (b) is a binding assay or a biochemical assay.

-   DD1. A method for analyzing an analyte in a vapor condensate sample     comprising:     obtaining a device of any prior device claim;     depositing the vapor condensate sample onto one or both pates of the     device;     placing the plates in a closed configuration and applying an     external force over at least part of the plates; and     analyzing the analytes in the layer of uniform thickness while the     plates are the closed configuration.

-   DD2. The method of any prior DD embodiment, wherein the method     comprises:

(a) obtaining a sample;

(b) obtaining a first and second plates that are movable relative to each other into different configurations, wherein each plate has a sample contact surface that is substantially planar, one or both plates are flexible, and one or both of the plates comprise spacers that are fixed with a respective sample contacting surface, and wherein the spacers have:

-   -   i. a predetermined substantially uniform height,     -   ii. a shape of pillar with substantially uniform cross-section         and a flat top surface;     -   iii. a ratio of the width to the height equal or larger than         one;     -   iv. a predetermined constant inter-spacer distance that is in         the range of 10 □m to 200 □m;     -   v. a filling factor of equal to 1% or larger;

(c) depositing the sample on one or both of the plates when the plates are configured in an open configuration, wherein the open configuration is a configuration in which the two plates are either partially or completely separated apart and the spacing between the plates is not regulated by the spacers;

(d), after (c), using the two plates to compress at least part of the sample into a layer of substantially uniform thickness that is confined by the sample contact surfaces of the plates, wherein the uniform thickness of the layer is regulated by the spacers and the plates, and has an average value equal to or less than 30 um with a variation of less than 10%, wherein the compressing comprises:

bringing the two plates together; and

conformable pressing, either in parallel or sequentially, an area of at least one of the plates to press the plates together to a closed configuration, wherein the conformable pressing generates a substantially uniform pressure on the plates over the at least part of the sample, and the pressing spreads the at least part of the sample laterally between the sample contact surfaces of the plates, and wherein the closed configuration is a configuration in which the spacing between the plates in the layer of uniform thickness region is regulated by the spacers; and

(e) analyzing the in the layer of uniform thickness while the plates are the closed configuration;

wherein the filling factor is the ratio of the spacer contact area to the total plate area; wherein a conformable pressing is a method that makes the pressure applied over an

area is substantially constant regardless the shape variation of the outer surfaces of the plates; and

wherein the parallel pressing applies the pressures on the intended area at the same time, and a sequential pressing applies the pressure on a part of the intended area and gradually move to other area.

-   DD3. The method of any prior DD embodiment, wherein the method     comprises:     -   removing the external force after the plates are in the closed         configuration; and imaging the analytes in the layer of uniform         thickness while the plates are the closed configuration; and     -   counting a number of analytes or the labels in an area of the         image. -   DD4. The method of any prior DD embodiment, wherein the method     comprises removing the external force after the plates are in the     closed configuration; and measuring optical signal in the layer of     uniform thickness while the plates are the closed configuration. -   DD5. The method of any prior DD embodiment, wherein the inter-spacer     distance is in the range of 20 □m to 200 □m. -   DD6. The method of any prior DD embodiment, wherein the inter-spacer     distance is in the range of 5 □m to 20 □m. -   DD7. The method of any prior DD embodiment, wherein a product of the     filling factor and the Young's modulus of the spacer is 2 MPa or     larger. -   DD8. The method of any prior DD embodiment, the surface variation is     less than 50 nm. -   DD9. The method of any prior DD embodiment, further comprising a     step of calculating the concentration of an analyte in the relevant     volume of sample, wherein the calculation is based on the relevant     sample volume defined by the predetermined area of the storage site,     the uniform sample thickness at the closed configuration, and the     amount of target entity detected. -   DD10. The method of any prior DD embodiment, wherein the analyzing     step comprise counting the analyte in the sample. -   DD11. The method of any prior DD embodiment, wherein the imaging and     counting is done by:

i. illuminating the cells in the layer of uniform thickness;

ii. taking one or more images of the cells using a CCD or CMOS sensor;

iii. identifying cells in the image using a computer; and

iv. counting a number of cells in an area of the image.

-   DD12. The method of any prior DD embodiment, wherein the external     force is provided by human hand. -   DD13. The method of any prior DD embodiment, wherein it future     comprises a dry reagent coated on one or both plates. -   DD14. The method of any prior DD embodiment, wherein the layer of     uniform thickness sample has a thickness uniformity of up to +/−5%. -   DD15. The method of any prior DD embodiment, wherein the spacers are     pillars with a cross-sectional shape selected from round, polygonal,     circular, square, rectangular, oval, elliptical, or any combination     of the same. -   DD16. The method of any prior DD embodiment, wherein the spacing     between the spacers is approximately the minimum dimension of an     analyte. -   EE1. The method of any prior CC or DD embodiment, wherein one or     both plate sample contact surfaces comprises one or a plurality of     amplification sites that are each capable of amplifying a signal     from the analyte or a label of the analyte when the analyte or label     is within 500 nm from an amplification site. -   EE2. The method of any prior CC or DD embodiment, wherein the sample     is exhale breath condensate. -   EE3. The method of any prior CC or DD embodiment, wherein the sample     is a vapor from a biological sample, an environmental sample, a     chemical sample, or clinical sample. -   EE4. The method of any prior CC or DD embodiment, wherein the     analyte comprises a molecule (e.g., a protein, peptides, DNA, RNA,     nucleic acid, or other molecules), cells, tissues, viruses, and     nanoparticles with different shapes. -   EE5. The method of any prior CC or DD embodiment, wherein the     analyte comprises volatile organic compounds (VOCs). -   EE6. The method of any prior CC or DD embodiment, wherein the     analyte comprises nitrogen, oxygen, CO2, H2O, and inert gases. -   EE7. The method of any prior CC or DD embodiment, wherein the     analyte is stained. -   EE8. The method of any prior CC or DD embodiment, wherein on one of     the sample surface, it further comprises an enclosure-spacer that     encloses a partial or entire VC samples deposited on the collection     plate. -   EE9. The method of any prior CC or DD embodiment, wherein the highly     uniform thickness has a value equal to or less than 0.5 um. -   EE10. The method of any prior CC or DD embodiment, wherein the     highly uniform thickness has a value in the range of 0.5 um to 1 um. -   EE11. The method of any prior CC or DD embodiment, wherein the     highly uniform thickness has a value in the range of 1 um to 2 um. -   EE12. The method of any prior CC or DD embodiment, wherein the     highly uniform thickness has a value in the range of 2 um to 10 um. -   EE13. The method of any prior CC or DD embodiment, wherein the     highly uniform thickness has a value in the range of 10 um to 20 um. -   EE14. The method of any prior CC or DD embodiment, wherein the     highly uniform thickness has a value in the range of 20 um to 30 um.     Biomarks and Applications

Further aspects of the present disclosure include a CROF device that includes a plurality of capture agents that each binds to a plurality of analytes in a sample, i.e., a multiplexed CROF device. In such instances, the CROF device containing a plurality of capture agents can be configured to detect different types of analytes (protein, nucleic acids, antibodies, etc.). The different analytes can be distinguishable from each other on the array based on the location within the array, the emission wavelength of the detectable label that binds to the different analytes, or a combination of the above.

Other pathogens that can be detected in a diagnostic sample using the devices, systems and methods in the present invention include, but are not limited to: Varicella zoster, Staphylococcus epidermidis, Escherichia coli, methicillin-resistant Staphylococcus aureus (MSRA), Staphylococcus aureus, Staphylococcus hominis, Enterococcus faecalis, Pseudomonas aeruginosa, Staphylococcus capitis, Staphylococcus wameri, Klebsiella pneumoniae, Haemophilus influenzae, Staphylococcus simulans, Streptococcus pneumoniae and Candida albicans; gonorrhea (Neisseria gorrhoeae), syphilis (Treponena pallidum), clamydia (Clamyda tracomitis), nongonococcal urethritis (Ureaplasm urealyticum), chancroid (Haemophilus ducreyi), trichomoniasis (Trichomonas vaginalis); Pseudomonas aeruginosa, methicillin-resistant Staphlococccus aureus (MSRA), Klebsiella pneumoniae, Haemophilis influenzae, Staphylococcus aureus, Stenotrophomonas maltophilia, Haemophilis parainfluenzae, Escherichia coli, Enterococcus faecalis, Serratia marcescens, Haemophilis parahaemolyticus, Enterococcus cloacae, Candida albicans, Moraxiella catarrhalis, Streptococcus pneumoniae, Citrobacter freundii, Enterococcus faecium, Kiebsella oxytoca, Pseudomonas fluorscens, Neiseria meningitidis, Streptococcus pyogenes, Pneumocystis carinii, Kiebsella pneumoniae Legionella pneumophila, Mycoplasma pneumoniae, and Mycobacterium tuberculosis, etc., as well as those listed in Tables B2 and 6.

TABLE B1 Diagnostic Markers Marker disease Aβ42, amyloid beta-protein (CSF) Alzheimer's disease. fetuin-A (CSF) multiple sclerosis. tau (CSF) niemann-pick type C. secretogranin II (CSF) bipolar disorder. prion protein (CSF) Alzheimer disease, prion disease Cytokines (CSF) HIV-associated neurocognitive disorders Alpha-synuclein (CSF) parkinsonian disorders (neuordegenerative disorders) tau protein (CSF) parkinsonian disorders neurofilament light chain (CSF) axonal degeneration parkin (CSF) neuordegenerative disorders PTEN induced putative kinase 1 (CSF) neuordegenerative disorders DJ-1 (CSF) neuordegenerative disorders leucine-rich repeat kinase 2 (CSF) neuordegenerative disorders mutated ATP13A2 (CSF) Kufor-Rakeb disease Apo H (CSF) parkinson disease (PD) ceruloplasmin (CSF) PD Peroxisome proliferator-activated receptor PD gamma coactivator-1 alpha (PGC-1α)(CSF) transthyretin (CSF) CSF rhinorrhea (nasal surgery samples) Vitamin D-binding Protein (CSF) Multiple Sclerosis Progression proapoptotic kinase R (PKR) and its AD phosphorylated PKR (pPKR) (CSF) CXCL13 (CSF) multiple sclerosis IL-12p40, CXCL13 and IL-8 (CSF) intrathecal inflammation Dkk-3 (semen) prostate cancer p14 endocan fragment (blood) Sepsis: Endocan, specifically secreted by activated-pulmonary vascular endothelial cells, is thought to play a key role in the control of the lung inflammatory reaction. Serum (blood) neuromyelitis optica ACE2 (blood) cardiovascular disease autoantibody to CD25 (blood) early diagnosis of esophageal squamous cell carcinoma hTERT (blood) lung cancer CAI25 (MUC 16) (blood) lung cancer VEGF (blood) lung cancer sIL-2 (blood) lung cancer Osteopontin (blood) lung cancer Human epididymis protein 4 (HE4) (blood) ovarian cancer Alpha-Fetal Protein (blood) pregnancy Albumin (urine) diabetics albumin (urine) uria albuminuria microalbuminuria kidney leaks AFP (urine) mirror fetal AFP levels neutrophil gelatinase-associated lipocalin Acute kidney injury (NGAL) (urine) interleukin 18 (IL-18) (urine) Acute kidney injury Kidney Injury Molecule -1 (KIM-1) (urine) Acute kidney injury Liver Fatty Acid Binding Protein (L-FABP) Acute kidney injury (urine) LMP1 (saliva) Epstein-Barr virus oncoprotein (nasopharyngeal carcinomas) BARF1 (saliva) Epstein-Barr virus oncoprotein (nasopharyngeal carcinomas) IL-8 (saliva) oral cancer biomarker carcinoembryonic antigen (CEA) (saliva) oral or salivary malignant tumors BRAF, CCNI, EGRF, FGF19, FRS2, GREB1, Lung cancer and LZTS1 (saliva) alpha-amylase (saliva) cardiovascular disease carcinoembryonic antigen (saliva) Malignant tumors of the oral cavity CA 125 (saliva) Ovarian cancer IL8 (saliva) spinalcellular carcinoma. thioredoxin (saliva) spinalcellular carcinoma. beta-2 microglobulin levels - monitor activity HIV of the virus (saliva) tumor necrosis factor-alpha receptors - HIV monitor activity of the virus (saliva) CA15-3 (saliva) breast cancer

TABLE B2 Diagnostic Markers  HPA axis activity (Cushing's disease, Adrenal cortex diseases, etc.): Cortisol  Pregnancy/fetal development: Progesterone, human chorionic gonadotropin,  Levonorgestrel, alpha-fetoprotein, early conception factor, Unconjugated Estriol, Estradiol,  interleukin-6, Inhibin-A  Infant development: NGAL, KIM-1, Cys-C, and B2mG, AFP, S100B, MBP  Menopause: Follicle stimulating hormone (FSH), Estrogen and progesterone, testosterone,  free testosterone, and dehydroepiandrosterone sulfate (DHEAS), cortisol and  dehydroepiandrosterone (DHEA)  Polycystic ovary syndrome: testosterone  Andropause: testosterone; testosterone precursors such as pregnenolone, progesterone,  17-hydroxypregnenolone, 17-hydroxyprogesterone, dehydroepiandrosterone (DHEA) and  delta-4-androstene-3,17-dione; testosterone and dihydrotestosterone metabolites such as the  17-ketosteroids androsterone and etiocholanolone, polar metabolites in the form of diols,  triols, and conjugates, as well as estradiol, estrogens, androsteindione, cortisol, FSH (follicle  stimulating hormone), LH (luteinizing hormone), and GnRH (gonadotropin-releasing hormone)  Coagulation status/disorders: b-Thromboglobulin, Platelet factor 4, Von Willebrand factor,  Factor I: Fibrinogen, Factor II: Prothrombin, Factor III: Tissue factor, Factor IV: Calcium,  Factor V: Proaccelerin, Factor VI, Factor VII: Proconvertin, Factor VIII:, Anti-hemolytic factor,  Factor IX: Christmas factor, Factor X: Stuart-Prower factor, Factor XI: Plasma thromboplastin  antecedent, Factor XII: Hageman factor, Factor XIII: Fibrin-stabilizing factor, Prekallikrein,  High-molecular-weight kininogen, Protein C, Protein S, D-dimer, Tissue plasminogen  activator, Plasminogen, a2-Antiplasmin, Plasminogen activator inhibitor 1 (PAI1)  Autism: miR-484, miR-21, miR-212, miR-23a, miR-598, miR-95, miR-129, miR-431, miR-7,  miR-15a, miR-27a, miR-15b, miR-148b, miR-132, or miR-128; miR-93, miR-106a, miR-539,  miR-652, miR-550, miR-432, miR-193b, miR-181d, miR-146b, miR-140, miR-381, miR-320a,  or miR-106b; GM1, GD1a, GD1b, or GT1b; Ceruloplasmin, Metalothioneine, Zinc, Copper,  B6, B12, Glutathione, Alkaline phosphatase, and Activation of apo-alkaline phosphatases  Alzheimer's Disease: miR-107, miR-29a, miR-29b-1, or miR-9; miR-128; HIF-la, BACE1,  Reelin, CHRNA7, or 3Rtau/4Rtau, Reelin, Cystatin C, Truncated Cystatin C, C3a, t-Tau,  Complement factor H, or alpha-2-macroglobulin; β-amyloid(1-42), β-amyloid(1-40), tau,  phosphor-tau-181, acetylcholinesterase enzyme (AChE), GSK-3, PKC, VCAM-1 and ICAM-1,  macrophage inflammatory proteins-1δ and -4 (MIP1δ and MIP4), regulated upon activation  normal T-cell (RANTES), tumor necrosis factor-alpha (TNFα), midregional pro-atrial  natriuretic peptide (MR-proANP), AD-associated neuronal thread protein (AD7c-NTP)  Parkinson's Disease: miR-133b; Nurr1, BDNF, TrkB, gstml, or 5100 beta; apo-H,  Ceruloplasmin, BDNF, Beta2-microglobulin, apoAll, tau, ABetal-42, DJ-1, cTnl, myoglobin,  MMP-9, MMP-8, MMP-2, sICAM-1, myeloperoxidase [MPO], IL-4, and/or IL-5; B-type  natiuretic peptide [BNP], IL-1α, IL-11, IL-10, TNF-α, IFN-γ, VEGF, insulin, GLP-1 (active),  GLP-1 (total), TREM1, Leukotriene E4, Akt1, Aβ-40, Aβ-42, Fas ligand, PSA, G-CSF, MIP-1α,  IL-22, IL-8, IL-21, IL-15, IL-6, IL-7, GM-CSF, IL-2, IL-12, IL-17α, IL-1β, MCP, IL-32 or  RANTES, apolipoproteins A1, D and E, ischemia-modified albumin (IMA), fibronectin, s.  alpha-amylase, aspartate aminotransferase, lactate dehydrogenase, tissue factor activity,  MCP-1, sVCAM-1, sCD-40, insulin-like growth factor I (IGF-I), IGF-II  Schizophrenia: miR-181b; miR-7, miR-24, miR-26b, miR-29b, miR-30b, miR-30e, miR-92, or  miR-195; IFITM3, SERPINA3, GLS, or ALDH7A1BASP1; TP5B, ATP5H, ATP6V1B, DNM1,  NDUFV2, NSF, PDHB  Bipolar disease: FGF2, ALDH7A1, AGXT2L1, AQP4, or PCNT2  Mood disorder: Mbp, Edg2, Fgfrl, Fzd3, Mag, Pmp22, Ugt8, Erbb3, Igfbp4, Igfbp6, Pde6d,  Ptprm, Nefh, Atp2c1, Atxn1, Btgl, C6orf182, Dicer1, Dnajc6, and Ednrb  Major Depressive Disorder: FGFR1, FGFR2, FGFR3, or AQP4, Secretogranin, VGF,  Cortisol, EGF, GCS, PPY, ACTH, AVP, CRH, MAT, A2M, ApoC3, CD4OL, IL-6, IL-13, IL-18,  IL-1 ra, MPO, PAI-1, TNFA, ACRP30, ASP, FABP, INS, LEP, PRL, RETN, Testosterone,  TSH, BDNF, S100B, NTF3, GDNF, ARTN  Prion disease: Amyloid B4, App, IL-1R1, or SOD1; PrP(c), 14-3-3, NSE, S-100, Tau, AQP-4  Inflammation: TNF-α, IL-6, IL1β, Rheumatoid factor (RF), Antinuclear Antibody (ANA), acute  phase markers including C-reactive protein (CRP), Clara Cell Protein (Uteroglobin); 14-3-3  protein epsilon; Isoform Long of Protocadherin alpha C2 precursor; Insulin-like growth factor  IA precursor; Isoform 1 of Protocadherin-8 precursor; Isoform 1 of Sodium/potassium/calcium  exchanger 2 precursor; Complement factor H-related 5; Di-N-acetylchitobiase precursor;  Isoform 1 of Protein NDRG2; N-acetylglucosamine-6-sulfatase precursor; Isoform 1 of  Semaphorin-3B precursor; Cadherin-5 precursor; UPF0454 protein Cl2orf49 precursor;  Dihydrolipoyl dehydrogenase, mitochondrial precursor; Metallothionein-3; Fas apoptotic  inhibitory molecule 2; Coactosin-like protein; Isoform Long of Platelet-derived growth factor A  chain Precursor; Isoform Long of Endothelin-3 precursor; HLA class I histocompatibility  antigen, A-1 alpha chain Precursor; Neuronal pentraxin-2 precursor; retbindin isoform 2;  Neuroendocrine convertase 2 precursor; 15 kDa selenoprotein isoform 1 precursor;  Phospholipase D4; Isoform 1 of CD109 antigen precursor; Ectonucleotide  pyrophosphatase/phosphodiesterase family; member 6 precursor; Fascin; Golgi  phosphoprotein 2; Isoform Delta 6 of Calcium/calmodulin-dependent protein kinase type II  delta chain; Isoform 1 of FRAS1-related extracellular matrix protein 2 Precursor; Putative  uncharacterized protein LOC130576; Isoform 1 of L-lactate dehydrogenase A chain; Isoform  1 of Polypeptide N-acetylgalactosaminyltransferase 13; Papilin; Protein DJ-1; Beta-  mannosidase precursor; Protein YIPF3; Isoform 1 of Receptor-type tyrosine-protein  phosphatase N2 Precursor; Cell growth regulator with EF hand domain protein 1; Sulfhydryl  oxidase 2 precursor; Ig lambda chain V-II region TRO; Ig lambda chain V-VI region AR; Ig  heavy chain V-III region WEA; Ig heavy chain V-III region CAM; Ig heavy chain V-III region  BUR; Myosin-reactive immunoglobulin kappa chain variable region (Fragment); Microfibrillar  protein 2 (Fragment); Ig kappa chain V-III region IARC/BL41 precursor; Ig kappa chain V-I  region Kue; Ig kappa chain V-I region Sew; Ig kappa chain V-III region B6; IGLV6-57 protein;  hypothetical protein L0C402665; Isoform 1 of Proline-rich acidic protein 1 precursor;  Rheumatoid factor RF-ET13; Rheumatoid factor D5 heavy chain (Fragment); Uncharacterized  protein ENSP00000375027; Uncharacterized protein ENSP00000375043; Uncharacterized  protein ENSP00000375019; Isoform 1 of Protocadherin-1 precursor; Isoform 1 of Epithelial  discoidin domain-containing receptor 1 precursor; Serine protease HTRA1 precursor; Isoform  Delta of Poliovirus receptor-related protein 1 Precursor; chemokine (C—X—C motif) ligand  16; Plastin-2; 14-3-3 protein zeta/delta; Apolipoprotein C-I1 precursor; Brain-specific  angiogenesis inhibitor 1 precursor; Semaphorin-3G precursor; Fol listatin-related protein 3  precursor; Hepatocyte growth factor activator precursor; Isoform 1 of Contactin-associated  protein-like 2 precursor; Phosphoglycerate kinase 1; Gamma-enolase; Phosphoglycerate  mutase 2; Low affinity immunoglobulin gamma Fc region receptor III-A precursor; Isoform  Beta of Poliovirus receptor precursor; Serine protease inhibitor Kazal-type 6 precursor;  Isoform 1 of Chordin precursor; Out at first protein homolog precursor; Isoform 1 of  Carboxypeptidase B2 precursor; ROB02 isoform a Ig kappa chain V-III region POM; Isoform  1 of Protein-L-isoaspartate(D-aspartate) O-Methyltransferase CDNA F1145296 fis, clone  BRHIP3003340, moderately similar to Actin, alpha skeletal muscle 2; Isoform 1 of RGM  domain family member B precursor; Carboxypeptidase N subunit 2 precursor; Hypothetical  LOC284297; L-6, IL-17, PAR-3, IL-17, T1/ST2, JunD, 5-LO, LTA4H, MBP, PLP, or alpha-beta  crystalline; antithrombin III; a-2 glycoprotein 1, zinc; transthyretin (prealbumin); NADH  dehydrogenase (ubiquinone) 1 beta subcomplex, 2; neurotrimin; orosomucoid 1 precursor (a-  1-acid glycoprotein-1); leucine-rich a-2-glycoprotein; leucine-rich repeat protein; α-1-  antitrypsin  Chronique fatigue syndrome: Cortisol; Ig alpha-1 chain C region; Polymeric  immunoglobulin receptor; Protein S100-A7; Cystatin-C; Cystatin-B; 14-3-3 protein zeta/delta;  Zinc-alpha-2-glycoprotein (ZAG)  Sjögren's syndrome: IgA, IgG, IgM autoantibodies; IgA, lactoferrin and beta2-microglobulin;  lysozyme C, and cystatin C, amylase and carbonic anhydrase; Autoantibodies (SSA/Ro;  LA/SS-B)  Systemic lupus erythematosus (SLE): Autoantibodies (CDC25B, APOBEC3G, ARAF,  BCL2A1, CLK1, CREB1, CSNK1G1, CSNK2A1, CWC27, DLX4, DPPA2, EFHD2, EGR2,  ERCC2, EWSR1, EZH2, FES, FOS, FTHL17, GEM, GNA15, GNG4, HMGB2, HNRNPUL1,  HOXB6, ID2, IF135, IGF2BP3, IGHG1, JUNB, KLF6, LGALS7, LIN28A, MLLT3, NFIL3,  NRBF2, PABPC1, PATZ1, PCGF2, PPP2CB, PPP3CC, PRM1, PTK2, PTPN4, PYGB, RET,  RPL18A, RPS7, RRAS, SCEL, SH2B1, SMAD2, STAM, TAF9, TIE1, UBA3, VAV1, VVT1,  ZAP70, ZNRD1, KIT, C6orf93, RPL34, DOM3Z, COPG2, DNCL12, RRP41, FBX09,  RALBP1, PIA52, EEF1D, CONI, KATNB1, POLR2E, CCT3, KIAA0643, RPL37A, GTF2H2,  MAP2K5, CDK3, RPS6KA1, MARK4, MTO1, MGC42105, NFE2L2, WDR45L, STK4,  PFKFB3, NTRK3, MLF1, TRIM37, ACTL7B, RPL18A, CKS1B, TUBA1, NME6, SUCLA2,  IGHG1, PRKCBP1, BAG3, TCEB3, RPL15, 55X4, MAP2K7, EEF1G, RNF38, PHLDA2,  KCMF1, NUBP2, VPS45A, SSA/Ro, dsDNA, Smith, histones, thrombin)  CREST syndrome: Autoantibodies (centromere)  Systemic sclerosis: Autoantibodies (Type I topoisomerase)  Primary biliary cirrhosis: Autoantibodies (nucleoporin 62, Sp100 nuclear antigen,  nucleoporin 210kDa, mitochondria)  Cirrhosis: NLT; NLT, HBsAG, AST, YKL-40, Hyaluronic acid, TIMP-1, alpha 2 macroglobulin,  a-1-antitrypsin P1Z allele, haptoglobin, or acid phosphatase ACP AC  Autoimmune hepatitis: Autoantibodies (Liver kidney microsomal type 1, smooth muscle)  Celiac disease: Autoantibodies (tTG, actin)  Celiac disease Irritable Bowel Syndrome (IBS): Anti-IgA gliadin, REG1A, MMP3  Inflammatory bowel disease (IBD): Trypsinogen IV, SERT; II-16, II-1beta, II-12, TNF-alpha,  interferon gamma, II-6, Rantes, MCP-1, Resistin, or 5-HT  Ulcerative colitis: IFITM1, IFITM3, STAT1, STAT3, TAP1, PSME2, PSMB8, HNF4G, KLF5,  AQP8, APT2B1, SLC16A, MFAP4, CCNG2, SLC44A4, DDAH1, TOB1, 231152_at, MKNK1,  CEACAM7*, 1562836_at, CDC42SE2, PSD3, 231169_at, IGL@*, GSN, GPM6B, CDV3*,  PDPK1, ANP32E, ADAM9, CDH1, NLRP2, 215777_at, OSBPL1, VNN1, RABGAP1L,  PHACTR2, ASH1L, 213710_s_at, CDH1, NLRP2, 215777_at, OSBPL1, VNN1, RABGAP1L,  PHACTR2, ASH1, 213710_s_at, ZNF3, FUT2, IGHA1, EDEM1, GPR171, 229713_at,  L00643187, FLVCR1, SNAP23*, ETNK1, L00728411, POSTN, MUC12, HOXA5, SIGLEC1,  LARP5, PIGR, SPTBN1, UFM1, C6orf62, WDR90, ALDH1A3, F2RL1, IGHV1-69, DUOX2,  RAB5A, or CP; (P)ASCA  Hyperplastic Polyp: SLC6A14, ARHGEF10, ALS2, IL1RN, SPRy4, PTGER3, TRIM29,  SERPINB5, 1560327 at, ZAK, BAG4, TRIB3, TTL, FOXQ1  Psoriasis: miR-146b, miR-20a, miR-146a, miR-31, miR-200a, miR-17-5p, miR-30e-5p, miR-  141, miR-203, miR-142-3p, miR-21, or miR-106a; miR-125b, miR-99b, miR-122a, miR-197,  miR-100, miR-381, miR-518b, miR-524, let-7e, miR-30c, miR-365, miR-133b, miR-10a, miR-  133a, miR-22, miR-326, or miR-215; IL-20, VEGFR-1, VEGFR-2, VEGFR-3, or EGR1;  Dermatitis herpetiformis: Autoantibodies (eTG)  Miller-Fisher Syndrome: Autoantibodies (ganglioside GQ1B)  Wegener's granulomatosis: Autoantibodies (c-ANCA)  Neuropathies: Autoantibodies (ganglioside GD3, ganglioside GM1)  Microscopic polyangiitis: Autoantibodies (p-ANCA)  Polymyositis: Autoantibodies (Signal recognition particles)  Scleromyositis: Autoantibodies (exosome complex Signal recognition particles)  Myasthenia gravis: Autoantibodies (nicotinic acetylcholine receptor Signal recognition  particles, muscle-specific kinase (MUSK) Signal recognition particles)  Lambert-Eaton myasthenic syndrome: Autoantibodies (voltage-gated calcium channel  (P/Q-type))  Hashimoto's thyroiditis: Autoantibodies (thyroid peroxidase)  Graves' disease: Autoantibodies (TSH receptor)  Paraneoplastic cerebellar syndrome: Autoantibodies (Hu, Yo (cerebellar Purkinje Cells),  amphiphysin)  Encephalitis: Autoantibodies (voltage-gated potassium channel (VGKC), N-methyl-D-  aspartate receptor (NMDA))  Sydenham's chorea: Autoantibodies (basal ganglia neurons)  Neuromyelitis: Autoantibodies (aquaporin-4)  Allergies: Allergen-specific IgAs  Rheumatic disease: miR-146a, miR-155, miR-132, miR-16, or miR-181; HOXD10, HOXD11,  HOXD13, CCL8, LIM homeobox2, or CENP-E; TNFα Rheumatoid arthritis: Autoantibodies (Rheumatoid factor, cyclic citrullinated protein), ATP-  binding cassette, sub-family A, member 12 isoform b; ATP-binding cassette Al2;  apolipoprotein; B-100 precursor - human; complement component 3 precursor; alpha-2-  glycoprotein 1,zinc; Alpha-2-glycoprotein, zinc; serine (or cysteine) proteinase inhibitor, clade  A (alpha-1 antiproteinase, antitrypsin), member 2; Protease inhibitor 1-like; protease inhibitor  1 (alpha-1-antitrypsin)-like; group-specific component (vitamin D binding protein); hDBP;  serine (or cysteine) proteinase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member  1; Protease inhibitor (alpha-1-antitrypsin); protease inhibitor 1 (anti-elastase), alpha-1-  antitrypsin; Vitronectin precursor V65 subunit; A kinase anchor protein 9 isoform 2; retrovirus-  related hypothetical protein II - human retrotransposon LINE-1; nuclear receptor coactivator  RAP250; peroxisome proliferator-act; nuclear receptor coactivator RAP2; Ig kappa chain  NIG26 precursor ? human; Vitamin D-binding protein precursor (DBF) (Group-specific  component) (GC-globulin) (VDB) complement C4A precursor [validated] Human; guanine  nucleotide binding protein (G protein), gamma transducing activity polypeptide 1; nucleoporin  98kD isoform 4; nucleoporin 98kD; Nup98-Nup96 precursor; GLFG-repeat containing;  nucleoporin; vitronectin precursor; serum spreading factor; somatomedin B; complement 5-  protein; Alpha-1-antitrypsin precursor; HMG-BOX transcription; factor BBX; x 001; protein;  hect domain and RLD 2; calcium channel, voltage-dependent, L type, alpha 1C subunit;  Alpha-2-antiplasmin precursor (Alpha-2-plasmin inhibitor) (Alpha-2-PI) (Alpha-2-AP);  Neuronal PAS domain protein 2 (Neuronal PAS2) (Member of PAS protein 4) (M0P4);  Retinoic acid receptor gamma-2 (RAR-gamma-2) alpha-1-B-glycoprotein - human; Heparin  cofactor II precursor (HC-II) (Protease inhibitor leuserpin 2) (HLS2); Ig gamma-1 chain C  region; isocitrate dehydrogenase 3 (NAD+) alpha precursor; H-IDH alpha; isocitric  dehydrogenase; isocitrate dehydrogenase [NAD] sub- unit alpha, mitochondrial; NAD specific ICDH; NAD(H)-specific isocitrate dehydrogenase alpha subunit precursor; isocitrate  dehydrogenase (NAD+) alpha chain precursor; ferroxidase (EC 1.16.3.1) precursor [validated] - human; similar to zona pellucida binding protein; N-acetylneuraminic acid phosphate  synthase; sialic acid synthase; sialic acid phosphate synthase; triple functional domain  (PTPRF interacting); deleted in bladder cancer chromosome region candidate 1;  ceruloplasmin (ferroxidase); Ceruloplasmin; RAB3A interacting protein (rabin3)-like 1; talin 2;  similar to Ceruloplasmin precursor (Ferroxidase); orosomucoid 1 precursor; Orosomucoid-1  (alpha-1-acid glycoprotein-1); Ig lambda chain precursor - human; cold autoinflammatory  syndrome 1; chromosome 1 open reading frame 7; angio-tensin/vasopressin receptor; similar  to KIAA0913 protein; sodium channel, voltage-gated, type V, alpha polypeptide; hypothetical  protein FLJ10379; orosomucoid 2; alpha-1-acid glycoprotein, type 2; Ig alpha-1 chain C  region; corticosteroid binding globulin precursor; corticosteroid binding globulin; alpha-1 anti-  proteinase, antitrypsin; KV3M_HUMAN IG KAPPA CHAIN V-III REGION HIC PRECURSOR;  MUC_HUMAN Ig mu chain C region; similar to Ig gamma-2 chain C region; alpha-1-  antichymotrypsin, precursor; alpha-1-antichymotrypsin; Antichymotrypsin; thyroid hormone  receptor-associated protein, 240 kDa subunit; Ig heavy chain - human; Alpha-1-  antichymotrypsin precursor (ACT) hypothetical protein XP_173158; hypothetical protein  DKFZp434G2226; haptoglobin; Plasma protease C1 inhibitor precursor (C1Inh) (C1Inh)  Haptoglobin-1 precursor; leucine-rich alpha-2-glycoprotein; S-arrestin; S-antigen; NAD(P)H  dehydrogenase, quinone 2; NAD(P)H menadione oxidoreductase-1, di-oxin-inducible-2;  NAD(P)H menadione oxi-doreductase 2, dioxin-inducible; angiotensin precursor [validated] -  human; similar to KIAA1902 protein; similar to KIAA1728 protein; calpain 3 isoform d; calpain,  large polypep- tide L3; calpain p94, large [catalytic] subunit; muscle-specific calcium-activated  neutral protease 3 large subunit; asp (abnormal spindle)-like, microcephaly associated;  haptoglobin-related protein; Haptoglobin-related locus; Ig alpha-2 chain C region; hypothetical  protein DKFZp434P1818.1 - human (fragment); GC3_HUMAN Ig gamma-3 chain C region  (Heavy chain disease protein) (HDC)  Organ Rejection: miR-658, miR-125a, miR-320, miR-381, miR-628, miR-602, miR-629, or  miR-125a; miR-324-3p, miR-611, miR-654, miR-330_MM1, miR-524, miR-17-3p_MM1, miR-  483, miR-663, miR-5,6-5p, miR-326, miR-197_MM2, or miR-346; matix metalloprotein-9,  proteinase 3, or HNP  Bone turnover/Osteoporosis: Pyridinoline, deoxypyridinoline, collagen type 1 corss-linked  N-telopeptide (NTX), collagen type 1 corss-linked C-telopeptide (CTX), bone sialoprotein  (BSP), Tartrate-resistant acid phosphatase 5b, deoxypyridinium (D-PYR) and osteocalcin  (OC), hepatocyte growth factor and interleukin-1 beta, Osteocalcin, alkaline phosphatase,  bone-specific alkaline phosphatase, serum type 1 procollagen (C1NP, P1NP)  Jaw osteonecrosis: PTH, insulin, TNF-α, leptin, OPN, OC, OPG and IL6  Gaucher's disease: lyso-Gbl, Chitotriosidase and CCL18  Traumatic brain injury: apoA-1, S-100B, isoprostane, GFAP, NGAL, neuron-specific  enolase (NSE)  Septic shock: 15-Hydroxy-PG dehydrogenase (up), LAIR1 (up), NFKB1A (up), TLR2,  PGLYPR1, TLR4, MD2, TLR5, IFNAR2, IRAK2, IRAK3, IRAK4, PI3K, PI3KCB, MAP2K6,  MAPK14, NFKB1A, NFKB1, ILI R1, MAP2K1IP1, MKNK1, FAS, CASP4, GADD45B, SOCS3,  TNFSF10, TNFSF13B, OSM, HGF, IL18R1, IL-6, Protein-C,IL-1beta  Cancer: FEN-1; CEA, NSE, CA 19-9, CA 125, PSA, proGRP, SCC, NNMT, anti-p53  autoantibodies, Separase and DPPFV/Separase, SERPINA3; ACTB; AFM; AGT; AMBP;  APOF; AP0A2; APOC1; APOE; APOH; SERPINC1; C1QB; C3; C4BPA; C8G; C9;  SERPINA6; CD14; CP; CRP; CSK; F9; FGA; FGG; FLNA; FN1; GC; HRG; IF; IGFALS;  ITGA1; ITIH1; ITIH2; ITIH4; KLKB1; LPA; MLL; MRC1; MYL2; MYO6; ORM1; SERPINF1;  SERPINA1; SERPINA4; PROS1; QSCN6; RGS4; SAA4; SERPINA7; TF; TFRC; TTN; UBC;  ALMS1; ATRN; PDCD11; KIAA0433; SERPINA10; BCOR; C10orf18; YY1AP1; FLJ10006;  BDP1; SMARCAD1; MKL2; CHST8; MCPH1; MY018B; MICAL-L1; PGLYRP2; KCTD7;  MGC27165; A1BG; A2M; ABLIM1; ACTA1; AHSG; ANK3; APCS; AP0A1; AP0A4; APOB;  APOC3; APOL1; AZGP1; B2M; BF; C1R; C1S; C2; C4B; C5; C6; C7; C8A; C8B;  CDK5RAP2/CDK5RA2; CHGB; CLU; COMP; CORO1A; CPN1; CUL1; DET1; DSC1; F13A1;  F2; F5; FGB; GOLGA1; GSN; HBA1; HBB; HP; HPX; HSPA5; HUNK; IGFBP5; IGHG1;  IGLV4-3; KIF5C; KNG1; KRT1; KRT10; KRT9; LBP; LGALS3BP; LRG1; LUM; MMP14;  MYH4; NEB; NUCB2; ORM2; PF4V1; PIGR; PLG; PON1; PPBP; RBP4; RIMS1; RNF6;  SAA1; SEMA3D; SERPIND1; SERPINF2; SERPING1; SF3B1; SPINK1; SPP1; SPTB;  SYNE1; TAF4B; TBC1D1; TLN1; TMSB4X; TRIP11; TTR; UROC1; VTN; VWF; ZFHX2;  ZYX; PSA (total prostate specific antigen), Creatinine, Prostatic acid phosphatase, PSA  complexes, Prostrate-specific gene-1, CA 12-5, Carcinoembryonic Antigen (CEA), Alpha feto  protein (AFP), hCG (Human chorionic gonadotropin), Inhibin, CAA Ovarian C1824, CA 27.29,  CA 15-3, CAA Breast C1924, Her-2, Pancreatic, CA 19-9, CAA pancreatic, Neuron-specific  enolase, Angiostatin DcR3 (Soluble decoy receptor 3), Endostatin, Ep-CAM (MK-1), Free  Immunoglobulin Light Chain Kappa, Free Immunoglobulin Light Chain Lambda, Herstatin,  Chromogranin A, Adrenomedullin, Integrin, Epidermal growth factor receptor, Epidermal  growth factor receptor-Tyrosine kinase, Pro-adrenomedullin N-terminal 20 peptide, Vascular  endothelial growth factor, Vascular endothelial growth factor receptor, Stem cell factor  receptor, c-kit/KDR, KDR, and Midkine; Zinc α2-glycoprotein (ZAG)  Adenoma: SI, DMBT1, CFI*, AQP1, APOD, TNFR5F17, CXCL10, CTSE, IGHA1, SLC9A3,  5LC7A1, BATF2, SOCS1, DOCK2, NOS2A, HK2, CXCL2, IL15RA, P0U2AF1, CLEC3B,  ANI3BP, MGC13057, LCK*, C4BPA, HOXC6, GOLT1A, C2orf32, MORA, 240856_at,  50053, MEI53P1, HIPK1, GLS, CPLX1, 236045_x_at, GALC, AMN, CCDC69, CCL28,  CPA3, TRIB2, HMGA2, PLCL2, NR3C1, ElF5A, LARP4, RP5-1022P6.2, PHLDB2, FKBP1B,  INDO, CLDN8, CNTN3, PBEF1, 5LC16A9, CDC25B, TPSB2, PBEF1,1D4, GJB5, CHN2,  LIMCH1, or CXCL9; ABCA8, KIAA1199, GCG, MAMDC2, C2orf32, 229670_at, IGF1,  PCDH7, PRDX6, PCNA, COX2, or MUC6  Head and Neck cancer: IL-b, IL-6, IL-8, VEGF, MMP-9, TGF-β, TNF-α, MMP-7,  plasminogen activated (PA), uPA, IGF, or INF-2  Barrett's esophagus: miR-21, miR-143, miR-145, miR-194, or miR-215; S100A2, 5100A4;  p53, MUC1, MUC2  Lung cancer: miR-21, miR-205, miR-221 (protective), let-7a (protective), miR-137 (risky),  miR-372 (risky), or miR-122a (risky); miR-17-92, miR-19a, miR-92, miR-155, miR-191, or  miR-210; EGFR, PTEN, RRM1, RRM2, ABCB1, ABCG2, LRP, VEGFR2, VEGFR3, class III  b-tubulin; KRAS, hENT1; RLF-MYCL1, TGF-ALK, or CD74-ROS1, CCNI, EGFR, FGF19,  FRS2, and GREB1 LZTS, BRAF, FRS2, ANXA1, Haptoglobin Hp2, Zinc Alpha2-Glycoprotein,  Calprotectin, Porphyromonas catoniae 16S rRNA, Campylobacter showae 16S rRNA,  Streptocococcus salivaris 16S rRNA, Campylobacter rectus 16S rRNA, Veillonella parvula  16S rRNA, Kigella oralis 16S rRNA, and Granulicatella adiacens 16S rRNA  Pancreatic cancer: miR-221, miR-181a, miR-155, miR-210, miR-213, miR-181b, miR-222,  miR-181b-2, miR-21, miR-181b-1, miR-220, miR-181d, miR-223, miR-100-1/2, miR-125a,  miR-143, miR-10a, miR-146, miR-99, miR-100, miR-199a-1, miR-10b, miR-199a-2, miR-221,  miR-181a, miR-155, miR-210, miR-213, miR-181b, miR-222, miR-181b-2, miR-21, miR-181b-  1, miR-181c, miR-220, miR-181d, miR-223, miR-100-1/2, miR-125a, miR-143, miR-10a, miR-  146, miR-99, miR-100, miR-199a-1, miR-10b, miR-199a-2, miR-107, miR-103, miR-103-2,  miR-125b-1, miR-205, miR-23a, miR-221, miR-424, miR-301, miR-100, miR-376a, miR-125b-  1, miR-21, miR-16-1, miR-181a, miR-181c, miR-92, miR-15, miR-155, let-7f-1, miR-212, miR-  107, miR-024-1/2, miR-18a, miR-31, miR-93, miR-224, or let-7d; miR-148a, miR-148b, miR-  375, miR-345, miR-142, miR-133a, miR-216, miR-217 or miR-139; KRAS, CTNNLB1, AKT,  NCOA3, or B-RAF; BRCA2, PALB2, or p16, MBD3L2, KRAS, STIM2, DMXL2, ACRV1, DMD  and CABLES1,TK2, GLTSCR2, CDKL3, TPT1 and DPM1  Breast cancer: miR-21, miR-155, miR-206, miR-122a, miR-210, miR-155, miR-206, miR-  210, or miR-21; let-7, miR-10b, miR-125a, miR-125b, miR-145, miR-143, miR-16, miR-10b,  miR-125a; hsp70, MART-1, TRP, HER2, hsp70, MART-1, TRP, HER2, ER, PR, Class III b-  tubulin, or VEGFA; GAS5; ETV6-NTRK3; CAH6 (Carbonic anhydrase VI), K2C4 (Cytokeratin  4), CYTA (Cystatin A), FABP4 (Epid. Fatty acid binding prot.), IGHGI (Ig gamma-1 chain C  region), TRFL (Lactoferrin), BPIL1 (Bact. Perm.-increasing prot.-1), CYTC (Cystatin C), HPT  (Haptoglobin), PROF1 (Profilin-1), ZA2G (Zinc-alpha-2-glycoprotein), ENOA (A1pha enolase),  IGHA2 (Ig alpha-2 chain C region), IL-1 ra (Interleukin-1 receptor anatagonist protein  precursor), Sl0A7 (S100 calcium-binding protein A7), and SPLC2 (Short palate, lung and  nasel epith Carc. assoc. protein 2)  Ovarian cancer: c-erbB-2, cancer antigen 15-3, p53, HER2/neu (c-erbB-2), 47D10 antigen,  PTCD2, SLC25A20, NFKB2, RASGRP2, PDE7A, MLL, PRKCE, GPATC3, PRIC285 and  GSTA4, MIPEP, PLCB2, SLC25A19, DEF6, ZNF236, Cl8orf22, COX7A2, DDX11, TOP3A,  C9orf6, UFC1, PFDN2, KLRD1, LOC643641, HSP90AB1, CLCN7, TNFAIP2, PRKCE,  MRPL40, FBF1, ANKRD44, CCT5, USP40, UBXD4, LRCH1, MRPL4, SCCPDH, STX6,  LOC284184, FLJ23235, GPATC3, CPSF4, CREM, HIST1H1D, HPS4, FN3KRP, ANKRD16,  C8 orf16, ATF71P2, PRIC285, miR-200a, miR-141, miR-200c, miR-200b, miR-21, miR-200a,  miR-200b, miR-200c, miR-203, miR-205, miR-214, miR-199″, or miR-215; miR-199a, miR-  140, miR-145, miR-100, miR-let-7 cluster, or miR-125b-1; ERCC1, ER, TOPO1, TOP2A, AR,  PTEN, CD24 or EGFR; VEGFA, VEGFR2, CA 125  Prostate cancer: AGPAT1, B2M, BASP2, IER3,1L1B, miR-9, miR-21, miR-141, miR-370,  miR-200b, miR-210, miR-155, or miR-196a; miR-202, miR-210, miR-296, miR-320, miR-370,  miR-373, miR-498, miR-503, miR-184, miR-198, miR-302c, miR-345, miR-491, miR-513,  miR-32, miR-182, miR-31, miR-26a-1/2, miR-200c, miR-375, miR-196a-1/2, miR-370, miR-  425, miR-425, miR-194-1/2, miR-181a-1/2, miR-34b, let-71, miR-188, miR-25, miR-106b,  miR-449, miR-99b, miR-93, miR-92-1/2, miR-125a, or miR-141; let-7a, let-7b, let-7c, let-7d,  let-7g, miR-16, miR-23a, miR-23b, miR-26a, miR-92, miR-99a, miR-103, miR-125a, miR-  125b, miR-143, miR-145, miR-195, miR-199, miR-221, miR-222, miR-497, let-7f, miR-19b,  miR-22, miR-26b, miR-27a, miR-27b, miR-29a, miR-29b, miR-30_5p, miR-30c, miR-100,  miR-141, miR-148a, miR-205, miR-520h, miR-494, miR-490, miR-133a-1, miR-1-2, miR-218-  2, miR-220, miR-128a, miR-221, miR-499, miR-329, miR-340, miR-345, miR-410, miR-126,  miR-205, miR-7-1/2, miR-145, miR-34a, miR-487, or let-7b; miR-15a, miR-16-1, miR-143 or  miR-145; AR, PCA3; FASLG or TNFSF10; U50; ACSL3-ETV1, C150RF21-ETV1, FLJ35294-  ETV1, HERV-ETV1, TMPRSS2-ERG, TMPRSS2-ETV1/4/5, TMPRSS2-ETV4/5, SLC5A3-  ERG, SLC5A3-ETV1, SLC5A3-ETV5, KLK2-ETV4, kallikrein-2 (KLK2), C reactive protein  (CRP), cysteine-rich secretory protein 3 (CRI5P3) and chromogranin A (CHGA), comprises  prostatic acid phosphatase (PAP), lactate dehydrogenase (LDH), alkaline phosphatase  (ALP), PSA  Esophageal Cancer: PCA3, GOLPH2, SPINK1, TMPRSS2:ERG, miR-192, miR-194, miR-  21, miR-200c, miR-93, miR-342, miR-152, miR-93, miR-25, miR-424, or miR-151; miR-27b,  miR-205, miR-203, miR-342, let-7c, miR-125b, miR-100, miR-152, miR-192, miR-194, miR-  27b, miR-205, miR-203, miR-200c, miR-99a, miR-29c, miR-140, miR-103, miR-107  Gastric cancer: miR-106a, miR-21, miR-191, miR-223, miR-24-1, miR-24-2, miR-107, miR-  92-2, miR-214, miR-25, or miR-221; let-7a; RRM2, or surviving; EphA4  Gastrointestinal Stromal Tumor (GIST): DOG-1, PKC-theta, KIT, GPR20, PRKCQ, KCNK3,  KCNH2, SCG2, TNFRSF6B, or CD34; PDGFRA, c-kit  Colorectal carcinoma: miR-24-1, miR-29b-2, miR-20a, miR-10a, miR-32, miR-203, miR-  106a, miR-17-5p, miR-30c, miR-223, miR-126, miR-128b, miR-21, miR-24-2, miR-99b, miR-  155, miR-213, miR-150, miR-107, miR-191, miR-221, miR-20a, miR-510, miR-92, miR-513,  miR-19a, miR-21, miR-20, miR-183, miR-96, miR-135b, miR-31, miR-21, miR-92, miR-222,  miR-181b, miR-210, miR-20a, miR-106a, miR-93, miR-335, miR-338, miR-133b, miR-346,  miR-106b, miR-153a, miR-219, miR-34a, miR-99b, miR-185, miR-223, miR-211, miR-135a,  miR-127, miR-203, miR-212, miR-95, or miR-17-5p; miR-143, miR-145, miR-143, miR-126,  miR-34b, miR-34c, let-7, miR-9-3, miR-34a, miR-145, miR-455, miR-484, miR-101, miR-145,  miR-133b, miR-129, miR-124a, miR-30-3p, miR-328, miR-106a, miR-17-5p, miR-342, miR-  192, miR-1, miR-34b, miR-215, miR-192, miR-301, miR-324-5p, miR-30a-3p, miR-34c, miR-  331, or miR-148b; EFNB1, ERCC1, HER2, VEGF, or EGFR; AFRs, Rabs, ADAM10, CD44,  NG2, ephrin-B1, MIF, b-catenin, Junction, plakoglobin, glalectin-4, RACK1, tetrspanin-8,  FasL, TRAIL, A33, CEA, EGFR, dipeptidase 1, hsc-70, tetraspanins, ESCRT, TS, PTEN, or  TOPO1; GREM1, DDR2, GUCY1A3, TNS1, ADAMTS1, FBLN1, FLJ38028, RDX, FAM129A,  ASPN, FRMD6, MCC, RBMS1, SNA12, MEIS1, DOCK10, PLEKHC1, FAM126A, TBC1D9,  VWF, DCN, ROBO1, MSRB3, LATS2, MEF2C, IGFBP3, GNB4, RCN3, AKAP12, RFTN1,  226834_at, COL5A1, GNG2, NR3C1*, SPARCL1, MAB21L2, AXIN2, 236894_at, AEBP1,  AP1S2, C10orf56, LPHN2, AKT3, FRMD6, COL15A1, CRYAB, COL14A1, LOC286167, QKI,  VWVTR1, GNG11, PAPPA, or ELDT1; 227458_at, INDO, CXCL9, CCR2, CD38, RARRES3,  CXCL10, FAM26F, TNIP3, NOS2A, CCRL1, TLR8, IL18BP, FCRL5, SAMD9L, ECGF1,  TNFSF13B, GBPS, or GBP1; TMEM37*, IL33, CA4, CCDC58, CLIC6, VERSUSNL1, ESPN,  APCDD1, C13orf18, CYP4X1, ATP2A3, L00646627, MUPCDH, ANPEP, C1orf115,  HSD3B2, GBA3, GABRB2, GYLTL1B, LYZ, SP025, CDKN2B, FAM89A, MOGAT2,  SEMA6D, 229376_at, TSPAN5, IL6R, or SLC26A2  Melanoma: miR-19a, miR-144, miR-200c, miR-211, miR-324-5p, miR-331, or miR-374; miR-  9, miR-15a, miR-17-3p, miR-23b, miR-27a, miR-28, miR-29b, miR-30b, miR-31, miR-34b,  miR-34c, miR-95, miR-96, miR-100, miR-104, miR-105, miR-106a, miR-107, miR-122a, miR-  124a, miR-125b, miR-127, miR-128a, miR-128b, miR-129, miR-135a, miR-135b, miR-137,  miR-138, miR-139, miR-140, miR-141, miR-149, miR-154, miR-154#3, miR-181a, miR-182, miR-183, miR-184, miR-185, miR-189, miR-190, miR-199, miR-199b, miR-200a, miR-200b,  miR-204, miR-213, miR-215, miR-216, miR-219, miR-222, miR-224, miR-299, miR-302a,  miR-302b, miR-302c, miR-302d, miR-323, miR-325, let-7a, let-7b, let-7d, let-7e, or let-7g;  MUM-1, beta-catenin, or Nop/5/Sik; DUSP-1, Alix, hsp70, Gib2, Gia, moesin, GAPDH, malate  dehydrogenase, p120 catenin, PGRL, syntaxin-binding protein 1 & 2, septin-2, or WD-repeat  containing protein 1; H/ACA (U1071), SNORA11D  Head and neck cancer: miR-21, let-7, miR-18, miR-29c, miR-142-3p, miR-155, miR-146b,  miR-205, or miR-21; miR-494; HPV E6, HPV E7, p53, IL-8, SAT, H3FA3; EGFR, EphB4, or  EphB2; CHCHD7-PLAG1, CTNNB1-PLAG1, FHIT-HMGA2, HMGA2-NFIB, LIFR-PLAG1, or  TCEA1-PLAG1  Oral squamous cell carcinoma: p53 autoantibodies, defensing-1, IncRNAs (MEG-3,  MALAT-1, HOTAIR, NEAT-1, UCA) Cortisol, lactate dehydrogenase, Transferrin, cyclin D1,  Maspin, alpha-amylase, IL-8, TNF-α, IL-1, IL-6, Basic fibroblast growth factor, Statherin, Cyfra  21.1, TPA, CA125, Endothelin-1, IL-β, CD44, IGF-1, MMP-2, MMP-9, CD59, Catalase,  Profilin, S100A9/MRP14, M2BP, CEA, Carcinoma associated antigen CA-50, Salivary  carbonyls, Maspin, 8-oxoguanine DNA glycosylase, OGG1, Phosphorylated-Src, Ki-67, Zinc  finger protein 501 peptide, Hemopexin, Haptoglobin, Complement C3, Transthyretin,  α1-antitrypsin, Peroxidase, GST, SOD, 8-OHdG, Glutathione, MDA, miR-125a, miR-200a,  miR-31  Salivary gland tumors: Fibroblast growth factor 2 (FGF2) and fibroblast growth factor  receptor 1 (FGFR1)  Hepatocellular carcinoma: miR-221; et-7a-1, let-7a-2, let-7a-3, let-7b, let-7c, let-7d, let-7e,  let-7f-2, let-fg, miR-122a, miR-124a-2, miR-130a, miR-132, miR-136, miR-141, miR-142, miR-  143, miR-145, miR-146, miR-150, miR-155(BIC), miR-181a-1, miR-181a-2, miR-181c, miR-  195, miR-199a-1-5p, miR-199a-2-5p, miR-199b, miR-200b, miR-214, miR-223, or pre-miR-  594; miR-122, miR-100, or miR-10a; miR-198 or miR-145  Renal cell carcinoma: miR-141, miR-200; miR-28, miR-185, miR-27, miR-let-7f-2; laminin  receptor 1, betaig-h3, Galectin-1, a-2 Macroglobulin, Adipophilin, Angiopoietin 2, Caldesmon  1, Class 11 MHC-associated invariant chain (CD74), Collagen IV-al, Complement component,  Complement component 3, Cytochrome P450, subfamily IIJ polypeptide 2, Delta sleep-  inducing peptide, Fc g receptor 111a (CD16), HLA-B, HLA-DRa, HLA-DRb, HLA-SB, IFN-  induced transmembrane protein 3, IFN-induced transmembrane protein 1, or Lysyl Oxidase;  IF1 alpha, VEGF, PDGFRA; ALPHA-TFEB, NONO-TFE3, PRCC-TFE3, SFPQ-TFE3, CLTC-  TFE3, or MALAT1-TFEBf  Renal cell carcinoma: Akt, total Erk1/2, total Met, total GSK3b, total Hif1a, total p21, total  AMPKa1, total VEGF, total PIGF, total VEGFR-1/Flt-1, phosphorylated Akt, phosphorylated  Erk1/2, phosphorylated. Met, phosphorylated STAT3, phosphorylated GSK3b, and  phosphorylated AMPKa1  Cervical cancer: HPV E6, HPV E7, or p53  Thyroid cancer: AKAP-BRAF, CCDC6-RET, ERC1-RETM, GOLGA5-RET, HOOK3-RET,  HRH4-RET, KTN1-RET, NCOA4-RET, PCM1-RET, PRKARA1A-RET, RFG-RET, RFG9-  RET, Ria-RET, TGF-NTRK1, TPM3-NTRK1, TPM3-TPR, TPR-MET, TPR-NTRK1, TRIM24-  RET, TRIM27-RET or TRIM33-RET; PAX8-PPARy  Neuroblastoma: Neuron-specific enolase (NSE)  Glioblastoma: GFAP  Brain cancer: miR-21, miR-10b, miR-130a, miR-221, miR-125b-1, miR-125b-2, miR-9-2,  miR-21, miR-25, or miR-123; miR-128a, miR-181c, miR-181a, or miR-181b; GOPC-ROS1;  MGMT; EGFR  Blood Cancers: HOX11, TALI, LY1, LM01, or LM02; TTL-ETV6, CDK6-MLL, CDK6-TLX3,  ETV6-FLT3, ETV6-RUNX1, ETV6-TTL, MLL-AFF1, MLL-AFF3, MLL-AFF4, MLL-GAS7,  TCBA1-ETV6, TCF3-PBX1 or TCF3-TFPT, for acute lymphocytic leukemia (ALL); BCL11B-  TLX3, IL2-TNFRFS17, NUP214-ABL1, NUP98-CCDC28A, TAL1-STIL, or ETV6-ABL2, for T-  cell acute lymphocytic leukemia (T-ALL); ATIC-ALK, KIAA1618-ALK, MSN-ALK, MYH9-ALK,  NPM1-ALK, TGF-ALK or TPM3-ALK, for anaplastic large cell lymphoma (ALCL); BCR-ABL1,  BCR-JAK2, ETV6-EVI1, ETV6-MN1 or ETV6-TCBA1, for chronic myelogenous leukemia  (CML); CBFB-MYH11, CHIC2-ETV6, ETV6-ABL1, ETV6-ABL2, ETV6-ARNT, ETV6-CDX2,  ETV6-HLXB9, ETV6-PER1, MEF2D-DAZAP1, AML-AFF1, MLL-ARHGAP26, MLL-  ARHGEF12, MLL-CASC5, MLL-CBL, MLL-CREBBP, MLL-DAB21P, MLL-ELL, MLL-EP300,  MLL-EPS15, MLL-FNBP1, MLL-FOX03A, MLL-GMPS, MLL-GPHN, MLL-MLLT1, MLL-  MLLT11, MLL-MLLT3, MLL-MLLT6, MLL-MY01F, MLL-PICALM, MLL-SEPT2, MLL-SEPT6,  MLL-SORBS2, MYST3-SORBS2, MYST-CREBBP, NPM1-MLF1, NUP98-HOXA13,  PRDM16-EVI1, RABEP1-PDGFRB, RUNX1-EVI1, RUNX1-MDS1, RUNX1-RPL22, RUNX1-  RUNX1T1, RUNX1-SH3D19, RUNX1-USP42, RUNX1-YTHDF2, RUNX1-ZNF687, or TAF15-  ZNF-384, for AML; CCND1-FSTL3, for chronic lymphocytic leukemia (CLL); and FLIP1-  PDGFRA, FLT3-ETV6, KIAA1509-PDGFRA, PDE4DIP-PDGFRB, NIN-PDGFRB, TP53BP1-  PDGFRB, or TPM3-PDGFRB, for hyper eosinophilia/chronic eosinophilia; miR-23b, miR-24-1,  miR-146, miR-155, miR-195, miR-221, miR-331, miR-29a, miR-195, miR-34a, or miR-29c;  miR-15a, miR-16-1, miR-29 or miR-223; miR-128b, miR-204, miR-218, miR-331, miR-181b-1,  miR-17-92  B-Cell Chronic Lymphocytic Leukemia: miR-183-prec, miR-190, miR-24-1-prec, miR-33,  miR-19a, miR-140, miR-123, miR-10b, miR-15b-prec, miR-92-1, miR-188, miR-154, miR-217,  miR-101, miR-141-prec, miR-153-prec, miR-196-2, miR-134, miR-141, miR-132, miR-192, or  miR-181b-prec; miR-213, miR-220; ZAP70, AdipoR1; BCL3-MYC, MYC-BTG1, BCL7A-MYC,  BRWD3-ARHGAP20 or BTG1-MYC  B-cell lymphoma: miR-17-92 polycistron, miR-155, miR-210, or miR-21, miR-19a, miR-92,  miR-142 miR-155, miR-221 miR-17-92, miR-21, miR-191, miR-205, U50; miR-17-92, miR-  155, miR-210, or miR-21; A-myb, LMO2, JNK3, CD10, bcl-6, Cyclin D2, IRF4, Flip, or CD44;  CITTA-BCL6, CLTC-ALK, IL21R-BCL6, PIM1-BCL6, TFCR-BCL6, IKZF1-BCL6 or SEC31A-  ALK  Burkitt's lymphoma: pri-miR-155; MYC, TERT, NS, NP, MAZ, RCF3, BYSL, IDE3, CDC7,  TCL1A, AUTS2, MYBL1, BMP7, ITPR3, CDC2, BACK2, TTK, MME, ALOX5, or TOP1; BCL6,  KI-67; IGH-MYC, LCP1-BCL6  Endometrial cancer: miR-185, miR-106a, miR-181a, miR-210, miR-423, miR-103, miR-107,  or let-7c; miR-71, miR-221, miR-193, miR-152, or miR-30c; NLRP7, AlphaV Beta6 integrin  Uterine leiomyomas: let-7 family member, miR-21, miR-23b, miR-29b, or miR-197  Myelofibrosis: miR-190; miR-31, miR-150 and miR-95; miR-34a, miR-342, miR-326, miR-  105, miR-149, miR-147  Pheochromocytoma: Catecholamines (epinephrine, norepinephrine, adrenaline)  Kidney disease/injury: ADBP-26, NHE3, KIM-1, glutamyltransferase, N-acetyl-beta-D-  glucosaminidase, lysozyme, NGAL, L-FABP, bikunin, urea, prostaglandins, creatinine, alpha-  1-microglobulin, retinol binding protein, glutathione-S-transferases, adiponectin, beta-2-  macroglobuin, calbindin-D, cysteine-rich angiogenic inducer 61, endothelial/epithial growth  factors, alpha-1-acid glycoprotein (orosomucoid), prealbumin, modified albumin, albumin,  transferrin, alpha-1-lipoprotein, alpha-1-antitrypsin matrix metalloproteinases (MMPs), alpha-  1-fetoprotein, Tamm Horsfall protein, homoarginine, interleukin 18, monocyte chemotactic  protein-1 (MCP-1), Lipocalin, VCAN, NRP1, CCL2, CCL19, COL3A1, GZMM, alpha-  galactosidase, casein kinase 2, IP-10, Mig, I-TAC, MIP-lα, MIP-3α, and MIP-1β, alpha-2-  glycoprotein-Zinc, leucine-rich alpha-2-glycoprotein, uromodulin, Pacsin 2, hepcidin-20,  hepcidin-25, AIF-2, urinary type-IV collagen, lipocalin-type prostaglandin D synthase (L-  PGDS), urinary neutrophil gelatinase-associated lipocalin (uNGAL), Annexin Al, Rab23, Shh,  Ihh, Dhh, PTCH1, PTCH2, SMO, Gli1, Gli2, Gli3, TLR4, cystatin C, AQPI, AQP2, AQP3,  NKCC2, NaPill, DAHKSEVAHRFKD; [RNA:] SLC12A1, UMOD, vWF, MMPI, MMP3,  SLC22A6, SLC22A 8, SLC22A 12, podocin, cubulin, LRP2, AQP9, and albumin,  carcinoembryonic antigen (CEA), mucin, alpha-fetoprotein, tyrosinase, melanoma associated  antigen, mutated tumor protein 53, p21, PUMA, prostate-specific antigen (PSA) or  thyroglobulin, von Willebrand factor (VWF), thrombin, factor VIII, plasmin, fibrin, osteopontin  (SPP1), Rab23, Shh, Ihh, Dhh, PTCH1, PTCH2, SMO, Gli1, Gli2, Gli3  Liver failure/disease: Lactoferrin, uric acid, cortisol, alpha-amylase, Carnitine; Cholic Acid;  Chenodeoxycholic, Deoxycholic, Lithocholic, Glycocholic; Prostaglandin E2; 13,14-dihydro-15-  keto Prostaglandin A2; Prostaglandin B2; Prostaglandin F2a; 15-keto-Prostaglandin F2a; 6-  keto-Prostaglandin F1α; Thromboxane B2; 11-dehydro-Thromboxane B2; Prostaglandin D2;  Prostaglandin J2; 15-deoxy-Δl2,14-Prostaglandin J2; 11β-Prostaglandin F2α; 5(S)-  Hydroxyeicosatetraenoic acid; 5(S)-Hydroxyeicosapentaenoic acid; Leukotriene B4;  Leukotriene B5; Leukotriene C4; Leukotriene D4; Leukotriene E4; Leukotriene F4; 12(S)-  Hydroxyeicosatetraenoic acid; 12(S)-Hydroxyeicosapentaenoic acid; 15(S)-  Hydroxyeicosatetraenoic acid; 15(S)-Hydroxyeicosapentaenoic acid; Lipoxin A4; 8(S)-  Hydroxyeicosatetraenoic acid; 9-Hydroxyeicosatetraenoic acid; 11-Hydroxyeicosatetraenoic  acid; 8-iso-Prostaglandin F2α; 9-Hydroxyoctadecadienoic acid; 13-Hydroxyoctadecadienoic  acid; 20(S)-Hydroxyeicosatetraenoic acid; 9,10-Epoxyoctadecenoic acid; 12,13-  Epoxyoctadecenoic acid; 12,13-Dihydroxyoctadecenoic acid; 5,6-Epoxyeicosatrienoic acid;  11,12-Epoxyeicosatrienoic acid; 14,15-Epoxyeicosatrienoic acid; 5,6-Dihydroxyeicosatrienoic  acid; 8,9-Dihydroxyeicosatrienoic acid; 11,12-Dihydroxyeicosatrienoic acid; 14,15-  Dihydroxyeicosatrienoic acid; 14,15-Epoxyeicosatetraenoic acid; 17,18-  Epoxyeicosatetraenoic acid; 14,15-Dihydroxyeicosatetraenoic acid; 17,18-  Dihydroxyeicosatetraenoic acid; 19,20-Dihydroxydocosapentaenoic acid; diacetylspermine,  hemopexin, TLR4  Stroke: MMP9, S100-P, S100Al2, 5100A9, coag factor V, Arginasel, CA-IV, monocarboxylic  acid transporter, ets-2, ElF2alpha, cytoskeleton associated protein 4, N-formylpeptide  receptor, Ribonuclease2, N-acetylneuraminate pyruvate lyase, BCL-6, or Glycogen  phosphorylase  Heart failure/Cardiovascular health: 8-iso-prostaglandin F2α (8-iso-PGF2a), miR-195, miR-  208, miR-214, let-7b, let-7c, let-7e, miR-15b, miR-23a, miR-24, miR-27a, miR-27b, miR-93,  miR-99b, miR-100, miR-103, miR-125b, miR-140, miR-145, miR-181a, miR-191, miR-195,  miR-199a, miR-320, miR-342, miR-451, or miR-499; miR-1, miR-10a, miR-17-5p, miR-19a,  miR-19b, miR-20a, miR-20b, miR-26b, miR-28, miR-30e-5p, miR-101, miR-106a, miR-126,  miR-222, miR-374, miR-422b, or miR-423; MRP14, 0D69; CK-MB, cTnI (cardiac troponin),  CRP, BPN, IL-6, MCSF, CD40, CD4OL, SFRP-3, NT-proBNP, troponin T,  SKITHRIHWESASLL, AHKSEVAHRFK, uroguanylin, BNP, miR-378, miR-497, miR-21, miR-  99a, miR 29a, miR-30b, miR-29c, miR-331.3p, miR-19a, miR-22, miR-502.3, and miR-652;  IL-16, sFas, Fas ligand, MCP-3, HGF, CTACK, EOTAXIN, adiponectin, IL-18, TIMP.4,  TIMP.1, CRP, VEGF, and EGF, C-reactive protein (CRP); myoglobin (MYO), creatinine  kinase myocardial band (CK-MB), cardiac troponins (cTn), and myeloperoxidase; TNF-α, and  MMP-9; CD40  Vulnerable plaque: Amylase, L-6, MMP-9, PAPP-A, D-dimer, fibrinogen, Lp-PLA2, SCD40L,  11-18, oxLDL, GPx-1, MCP-1, P1GF, or CRP  High blood pressure: lysozyme  Fibromyalgia: NR2D  Neuropathic Pain: CCR2/4, CNP; ICAM-1, CGRP, TIMP-1, CLR-1, HSP-27, FABP, or  apolipoprotein D; OX42, ED9  Tiredness/fatigue: PPGKPQGPPPQGGNQPQGPPPPPGKPQ (SEQ ID NO: 1);  GNPQGPSPQGGNKPQGPPPPPGKPQ (SEQ ID NO: 2);  SPPGKPQGPPQQEGNKPQGPPPPGKPQ (SEQ ID NO: 3 [[//]]); GGHPPPP (SEQ ID NO:  4), ESPSLIA (SEQ ID NO: 5); endorepellin; human herpesvirus 6, human herpesvirus 7,  human cytomegalovirus, and Epstein-Barr virus (EBV)  Stress: Cortisol, chromogranin A, alpha-amylase, secretary IgA, lysozyme, dehydro-  androsteronesulfate; 17-ketosteroidsulfate; dehydro-epiandrostronesulfate; corticosteroid, 17-  hydroxycorticosteroid, growth hormone, oxytocin, aldose reductase, apoptosis signal-  regulating kinase 1, aquaporin 5, beta-endorphin, betaine GABA transporter, caspase  recruitment domain protein 9, caspase 8, cyclin D, cyclooxygenase 2, cytochrome P450,  cytochrome c, c-fos, c-jun, epidermal growth factor receptor, ferritin, glucocorticoid receptor,  glucose regulated protein 58, glucose regulated protein 75, glutathione 5-transferase p,  GroEL, heat shock protein 25/27, heat shock protein 40, heat shock protein 60, heat shock  protein 70, heat shock protein 90, heat shock transcription factor-1, heme oxygenase-1,  interleukin 1β, interleukin 6, interleukin 8, interleukin 10, interleukin 12, laminin, leptin  receptor, matrix metalloproteinase 9, metallothionein, Mek-1, Mekk-1, inducible nitric oxide  synthase, peripheral benzodiazepine receptor, p38 MAPK, salivary alpha amylase, SAPK,  serotonin, serotonin receptor, substance P, superoxide dismutase Mn, superoxide dismutase  Cu/Zn, superoxide dismutase EC, transforming growth factor β, tumor suppressor p53, and  vasoactive intestinal peptide  Malnutrition: sIgA  Nutritional status: Prealbumin, Albumin, Retinol-binding protein (RBP), Transferrin,  Acylation-Stimulating Protein (ASP), Adiponectin, Agouti-Related Protein (AgRP),  Angiopoietin-like Protein 4 (ANGPTL4, FIAF), C-peptide, AFABP (Adipocyte Fatty Acid  Binding Protein, FABP4), Acylation-Stimulating Protein (ASP), EFABP (Epidermal Fatty Acid  Binding Protein, FABP5), Glicentin, Glucagon, Glucagon-Like Peptide-1, Glucagon-Like  Peptide-2, Ghrelin, Insulin, Leptin, Leptin Receptor, PYY, RELMs, Resistin, and sTfR (soluble  Transferrin Receptor)  Energy balance (protein excretion)/energy status/metabolic state: AMPK, pre-albumin,  retinol binding protein, urea, cholesterol, lipoproteins, insulin, insulin C peptide, IGF binding  proteins, e.g. IGF-BPI, liver enzymes  Diabetes: 11-8, CTSS, ITGB2, HLA-DRA, CD53, PLAG27, or MMP9; RBP4; 8-iso-  prostaglandin F2α (8-iso-PGF2α), 11-dehydro-thromboxane B₂ (TXM), C-peptide, Advanced  glycosylation end products (AGEs), 1,5-anhydroglucitol, NGPTL3 and 4, autoantibodies (Zn  transporter 8, glutamic acid decarboxylase (GAD)), ATP-binding cassette, sub-family C  (CFTR/MRP), member 8; ATP-binding cassette, sub-family C (CFTR/MRP), member 9;  angiotensin I converting enzyme (peptidyl-dipeptidase A) 1; adenylate cyclase activating  polypeptide 1 (pituitary); adiponectin, C1Q and collagen domain containing; adiponectin  receptor 1; adiponectin receptor 2; adrenomedullin; adrenergic, beta-2-, receptor, surface;  advanced glycosylation end product-specific receptor; agouti related protein homolog  (mouse); angiotensinogen (serpin peptidase inhibitor, clade A, member 8); angiotensin II  receptor, type 1; angiotensin II receptor-associated protein; alpha-2-HS-glycoprotein; v-akt  murine thymoma viral oncogene homolog 1; v-akt murine thymoma viral oncogene homolog  2; albumin; Alstrom syndrome 1; archidonate 12-lipoxygenase; ankyrin repeat domain 23;  apelin, AGTRL 1 Ligand; apolipoprotein A-I; apolipoprotein A-II; apolipoprotein B (including  Ag(x) antigen); apolipoprotein E; aryl hydrocarbon receptor nuclear translocator; Aryl  hydrocarbon receptor nuclear translocator-like; arrestin, beta 1; arginine vasopressin  (neurophysin II, antidiuretic hormone, Diabetes insipidus, neurohypophyseal); bombesin  receptor subtype 3; betacellulin; benzodiazepine receptor (peripheral); complement  component 3; complement component 4A (Rodgers blood group); complement component  4B (Childo blood group); complement component 5; Calpain-10; cholecystokinin;  cholecystokinin (CCK)-A receptor; chemokine (C-C motif) ligand 2; CD14 molecule; CD163  molecule; CD36 molecule (thrombospondin receptor); CD38 molecule; CD3d molecule, delta  (CD3-TCR complex); CD3g molecule, gamma (CD3-TCR complex); CD40 molecule, TNF  receptor superfamily member 5; CD40 ligand (TNF superfamily, member 5, hyper-IgM  syndrome); CD68 molecule; cyclin-dependent kinase 5; complement factor D (adipsin);  CASP8 and FADD-like apoptosis regulator; Clock homolog (mouse); chymase 1, mast cell;  cannabinoid receptor 1 (brain); cannabinoid receptor 2 (macrophage); cortistatin; carnitine  palmitoyltransferase I; carnitine palmitoyltransferase II; complement component (3b/4b)  receptor 1; complement component (3d/Epstein Barr virus) receptor 2; CREB binding protein  (Rubinstein-Taybi syndrome); C-reactive protein, pentraxin-related; CREB regulated  transcription coactivator 2; colony stimulating factor 1 (macrophage); cathepsin B; cathepsin  L; cytochrome P450, family 19, subfamily A, polypeptide 1; Dio-2, death inducer-obliterator 1;  dipeptidyl-peptidase 4 (CD26, adenosine deaminase complexing protein 2); epidermal growth  factor (beta-urogastrone); early growth response 1; epididymal sperm binding protein 1;  ectonucleotide; pyrophosphatase/phosphodiesterase 1; E1A binding protein p300;  coagulation factor XIII, Al polypeptide; coagulation factor VIII, procoagulant component  (hemophilia A); fatty acid binding protein 4, adipocyte; Fas (TNF receptor superfamily,  member 6); Fas ligand (TNF superfamily, member 6); free fatty acid receptor 1; fibrinogen  alpha chain; forkhead box A2; forkhead box O1A; ferritin; glutamate decarboxylase 2; galanin;  gastrin; glucagon; glucokinase; gamma-glutamyltransferase 1; growth hormone 1;  ghrelin/obestatin preprohormone; gastric inhibitory polypeptide; gastric inhibitory polypeptide  receptor; glucagon-like peptide 1 receptor; guanine nucleotide binding protein (G protein),  beta polypeptide 3; glutamic-pyruvate transaminase (alanine aminotransferase); gastrin  releasing peptide (bombesin); gelsolin (amyloidosis, Finnish type); hemoglobin; hemoglobin,  beta; hypocretin (orexin); neuropeptide; precursor; hepatocyte growth factor (hepapoietin A;  scatter factor); hepatocyte nuclear factor 4, alpha; haptoglobin; hydroxysteroid (11-beta);  dehydrogenase 1; heat shock 70 kDa protein 1B; islet amyloid polypeptide; intercellular  adhesion molecule 1 (CD54), human rhinovirus receptor; interferon, gamma; insulin-like  growth factor 1 (somatomedin C); insulin-like growth factor 2 (somatomedin A); insulin-like  growth factor binding protein 1; insulin-like growth factor binding protein 3; inhibitor of kappa  light polypeptide gene enhancer in B-cells, kinase beta; interleukin 10; interleukin 18  (interferon-gamma-inducing factor); interleukin 1, alpha; interleukin 1, beta; interleukin 1  receptor antagonist; interleukin 2; interleukin 6 (interferon, beta 2); interleukin 6 receptor;  interleukin 8; inhibin, beta A (activin A, activin AB alpha polypeptide); insulin; insulin receptor;  insulin promoter factor-1; insulin receptor substrate 1; insulin receptor substrate-2; potassium  inwardly-rectifying channel, subfamily J, member 11; potassium inwardly-rectifying channel,  subfamily J, member 8; klotho; kallikrein B, plasma (Fletcher factor) 1; leptin (obesity  homolog, mouse); leptin receptor; legumain; lipoprotein, Lp(a); lipoprotein lipase; v-maf  musculoaponeurotic brosarcoma oncogene homolog A (avian); mitogen-activated protein  kinase 8; interacting protein 1; mannose-binding lectin (protein C) 2, soluble (opsonic defect);  melanocortin 4 receptor; melanin-concentrating hormone receptor 1; matrix metallopeptidase  12 (macrophage elastase); matrix metallopeptidase 14 (membrane-inserted); matrix  metallopeptidase 2 (gelatinase A, 72 kDa gelatinase, 72 kDa type IV collagenase); matrix  metallopeptidase 9 (gelatinase B, 92 kDa gelatinase, 92 kDa type IV collagenase); nuclear  receptor co-repressor 1; neurogenic differentiation 1; nuclear factor of kappa light polypeptide  gene enhancer in B-cells 1(p105); nerve growth factor, beta polypeptide; non-insulin-  dependent Diabetes Mellitus (common, type 2) 1; non-insulin-dependent Diabetes Mellitus  (common, type 2) 2; Noninsulin-dependent Diabetes Mellitus 3; nischarin (imidazoline  receptor); NF-kappaB repressing factor; neuronatin; nitric oxide synthase 2A; Niemann-Pick  disease, type 02; natriuretic peptide precursor B; nuclear receptor subfamily 1, group D,  member 1; nuclear respiratory factor 1; oxytocin, prepro-(neurophysin I); purinergic receptor  P2Y, G-protein coupled, 10; purinergic receptor P2Y, G-protein coupled, 12; purinergic  receptor P2Y, G-protein coupled, 2; progestagen-associated endometrial; protein (placental  protein 14, pregnancy-associated endometrial alpha-2-globulin, alpha uterine protein); paired  box gene 4; pre-B-cell colony enhancing factor 1; phosphoenolpyruvate carboxykinase 1  (PEPCK1); proprotein convertase; subtilisin/kexin type 1; placental growth factor, vascular;  endothelial growth factor-related protein; phosphoinositide-3-kinase, catalytic, alpha  polypeptide; phosphoinositide-3-kinase, regulatory subunit 1 (p85 alpha); phospholipase A2,  group XIIA; phospholipase A2, group IID; plasminogen activator, tissue; patatin-like  phospholipase domain containing 2; proopiomelanocortin (adrenocorticotropin/beta-  lipotropin/alpha-melanocyte stimulating hormone/beta- melanocyte stimulating  hormone/beta-endorphin); paraoxonase 1 ESA, PON, Paraoxonase; peroxisome proliferative  activated receptor, alpha; peroxisome proliferative activated receptor, delta; peroxisome  proliferative activated receptor, gamma; peroxisome proliferative activated receptor, gamma,  coactivator 1; protein phosphatase 1, regulatory (inhibitor) subunit 3A (glycogen and  sarcoplasmic reticulum binding subunit, skeletal muscle); protein phosphatase 2A, regulatory  subunit B'(PR 53); protein kinase, AMP-activated, beta 1 non-catalytic subunit; protein kinase,  cAMP-dependent, catalytic, alpha; protein kinase C, epsilon; proteasome (prosome,  macropain) 26S subunit, non-ATPase, 9 (Bridge-1); prostaglandin E synthase; prostaglandin-  endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase); protein tyrosine  phosphatase, mitochondria! 1; Peptide YY retinol binding protein 4, plasma (RBP4);  regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein);  resistin; ribosomal protein S6 kinase, 90 kDa, polypeptide 1; Ras-related associated with  Diabetes; serum amyloid Al; selectin E (endothelial adhesion molecule 1); serpin peptidase  inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6; serpin peptidase inhibitor,  clade E (nexin, plasminogen activator inhibitor type 1), member 1; serum/glucocorticoid  regulated kinase; sex hormone-binding globulin; thioredoxin interacting protein; solute carrier  family 2, member 10; solute carrier family 2, member 2; solute carrier family 2, member 4;  solute carrier family 7 (cationic amino acid transporter, y+system), member 1(ERR); SNF1-  like kinase 2; suppressor of cytokine signaling 3; v-src sarcoma (Schmidt-Ruppin A-2) viral  oncogene homolog (avian); sterol regulatory element binding transcription factor 1; solute  carrier family 2, member 4; somatostatin receptor 2; somatostatin receptor 5; transcription  factor 1, hepatic; LF-B1, hepatic nuclear factor (HNF1); transcription factor 2, hepatic, LF-B3,  variant hepatic nuclear factor; transcription factor 7-like 2 (T-cell specific, HMG-box);  transforming growth factor, beta 1 (Camurati-Engelmann disease); transglutaminase 2 (C  polypeptide, protein-glutamine-gamma-glutamyltransferase); thrombospondin 1;  thrombospondin, type I, domain containing 1; tumor necrosis factor (TNF superfamily,  member 2); tumor necrosis factor (TNF superfamily, member 2); tumor necrosis factor  receptor superfamily, member 1A; tumor necrosis factor receptor superfamily, member 1B;  tryptophan hydroxylase 2; thyrotropin-releasing hormone; transient receptor potential cation  channel, subfamily V, member 1; thioredoxin interacting protein; thioredoxin reductase 2;  urocortin 3 (stresscopin); uncoupling protein 2 (mitochondria!, proton carrier); upstream  transcription factor 1; urotensin 2; vascular cell adhesion molecule 1; vascular endothelial  growth factor; vimentin; vasoactive intestinal peptide; vasoactive intestinal peptide receptor 1;  vasoactive intestinal peptide receptor 2; von VVillebrand factor; Wolfram syndrome 1  (wolframin); X-ray repair complementing defective repair in Chinese hamster cells 6; c-  peptide; cortisol; vitamin D3; estrogen; estradiol; digitalis-like factor; oxyntomodulin;  dehydroepiandrosterone sulfate (DHEAS); serotonin (5-hydroxytryptamine); anti-CD38  autoantibodies; gad65 autoantibody; Angiogenin, ribonuclease, RNase A family, 5;  Hemoglobin A1c; Intercellular adhesion molecule 3 (CD50); interleukin 6 signal transducer  (gp130, oncostatin M receptor); selectin P (granule embrane protein 140 kDa, antigen CD62);  TIMP metallopeptidase inhibitor; Proinsulin; endoglin;  interleukin 2 receptor, beta; insulin-like growth factor binding protein 2; insulin-like growth  factor 1 receptor; fructosamine, N-acetyl-beta-d-glucosaminidase, pentosidine, advanced  glycation end product, beta2-microglobulin, pyrraline  Metabolic syndrome/prediabetes: GFAP autoantibodies  Alcohol abuse/dependence: aminotransferases, gamma-glutamyltransferase, ethanol, ethyl  glucuronide, sialic acid, β-hexosaminidase A, oral peroxidase, methanol, diethylene/ethylene  glycol, α-amylase, clusterin, haptoglobin, heavy/light chains of immunoglobulins and  transferrin; α-fucosidase (FUC), α-mannosidase (MAN), β-galactosidase (GAL), and β-  glucuronidase (GLU)  Non-alcoholic fatty liver disease: cytokeratin CK-18 (M65 antigen), caspase-cleaved CK-18  (M30-antigen), resistin, adiponectin, visfatin, insulin, tumor necrosis factor-alpha (TNF-α),  interleukin 6 (IL-6), or interleukin 8 (IL-8), aspartate aminotransferase (AST) and alanine  aminotransferase (ALT); gamma-glutamyltransferase (GGT), immunoglobulin A,  carbohydrate-deficient transferrin (CDT), glutamic oxaloacetic transaminase (GOT), glutamic  pyruvic transaminase (GPT), bilirubin  Cystic fibrosis: amylase, cathepsin-D, lactate dehydrogenase  Ectodermal dysplasia: alpha-amylase  Sarcoidosis: IL-6, TNF-α, IFN-α, IL-17, IP-10, MIG, HGF, VEGF, TNF-RII, G-CSF, IFN-γ,  MCP-1, RANTES and IL-5  Asthma: eotaxin-1/CCL11, RANTES/CCL5, and IL-5; IL-1β, IL-6, MCP-1/CCL2, and IL-  8/CXCL8; IP-10/CXCL10  Periodontitis/dental caries: aspartate aminotransferase (AST) and alkaline phosphatase  (ALP), uric acid and albumin; 12-HETE; MMP-8, TIMP-1, and ICTP  Muscle damage: Myoglobin, creatine kinase (CK), lactate dehydrogenase (LDH), aldolase,  troponin, carbonic anhydrase type 3 and fatty acid-binding protein (FABP), transaminases  Infection (Mycobacterium tuberculosis): IL-32, NXNL1, PSMA7, C6orf61, EMP1, CLIC1,  LACTB and DUSP3, L0C389541, MIDI IP 1, KLRC3, KLF9, FBXQ32, C50RF29, CHUK ,  L00652062, C6ORF60, MTMR I I, sCD170; IFN-gamma; IL-I13, IL-6, IL-8, IL-10, IL-12p70,  sCD4, SCD25, SCD26, sCD32b/c, SCD50, SCD56, sCD66a, SCD83, sCD85j, SCD95,  SCD106, sCD120b, sCD121b, SCD127, SCD154, SCD222, SCD226, sCDw329 and TNF  alpha; VEGF, AAT, CRP, IL-IRA, TIMP-1, IL- 18, A2Macro, Haptoglobin ICAM-1, VCAM- 1,  SCF, IL-17, Fibrinogen, beta-2-macroglobulin, TNF-alpha, C3 and TNFR2, GPR117, TAZ,  HSDL I, HIP 1 (host)  Infection (Helicobacter pylori): MUC-5B and MUC 7  Infection (Candida species): Hsp70, calprotectin, histatins, mucins, basic proline rich  proteins and peroxidases (host);  Infection (influenza): Hemagglutinin (H1), neuraminidase (Ni); C-reactive protein, [RNA:]  DNA cross-link repair 1A, PS02 homolog, synaptonemal complex protein 3, v-maf  musculoaponeurotic fibrosarcoma oncogene family, chitinase 3-like 3, matrix  metalloproteinase 12, ATP-binding cassette, sub-family E (OABP), member 1, ATP-binding  cassette, sub-family F (GCN20), member 1, feminization 1 homolog a (C. elegans), general  transcription factor II H. polypeptide 2, forkhead box P1, zinc finger protein 282, arginyl-tRNA  synthetase-like, Mitochondrial ribosomal protein L48, ribosomal protein S4, X-linked,  eukaryotic translation elongation factor 1 alpha 1, proteaseome (prosome, macropain) 28  subunit 3, GLE1 RNA export mediator-like (yeast), small nuclear ribonucleoprotein  polypeptide A', cleavage and polyadenylation specific factor 2, ribosomal protein L27a, ,  thioredoxin domain containing 4 (endoplasmic reticulum), flap structure specific endonuclease  1, ADP-ribosylation factor-like 6 interacting protein 2, cytidine 5'-triphosphate synthase 2,  glutathione S-transferase, mu 5, phospholipase D1, aspartate-beta-hydroxylase, leukotriene  A4 hydrolase, cytochrome P450 family 17, subfamily a, polypeptide 1, thioredoxin interacting  protein, carbonyl reductase 2, alpha globin regulatory element containing gene, male-specific  lethal-2 homolog (Drosophila), RAB1, member RAS oncogene family, protein tyrosine  phosphatase, non-receptor type 21, potassium voltage-gated channel, lsk-related subfamily,  gene 3, BcI2-associated athanogene 3, lymphocyte cytosolic protein 2, pore forming protein-  like, tumor necrosis factor receptor superfamily, member 19, filamin beta, microtubule-actin  crosslinking factor 1, keratin complex 1, acidic, gene 18, keratin complex 1, acidic, gene 19,  mesoderm development candiate 2, tubulin, alpha 4? glutathione peroxidase 1, integrin  linked kinase, guanine nucleotide binding protein, alpha inhibiting 2, cyclin L2, tubulin, alpha  2, DEAD (Asp-Glu-Ala-Asp) box polypeptide 5, programmed cell death 4, proteasome  (prosome, macropain) 26S subunit, non-ATPase 8, signal sequence receptor, beta, RAD23b  homolog (host)  Infection (HIV-1): p24, gp41, gp120  Infection (Hepatitis B virus): Core, Envelope, Surface (Ay)  Infection (Hepatitis C virus): Core, NS3, NS4, NS5  Infection (Hepatitis E virus): 0rf2 3 KD, 0rf2 6 KD, 0rf3 3 KD  Infection (Vibrio cholerae): Cholera Toxin  Infection (Corynebacterium diphtheria): Diphtheria toxin  Infection (Epstein-Barr virus): EA, VCA, NA  Infection (Herpes simplex virus HSV-1): gD  Infection (Herpes simplex virus HSV-2): gG  Infection (Clostridium tetani): Tetanus toxin  Infection (Treponema pallidum): 15 kd, p47  Infection (Entamoeba histolytica): M17  Infection (Toxoplasma gondii): a2-HS glycoprotein and apB glycoprotein (host); TGME49  052280, TGME49_021500, TGME49J) 19630, TGME49_061720 and TGME49_076220  Infection (Dengue virus): IL-10, fibrinogen, C4A, immunoglobulin, tropomyosin, albumin,  SCSb-9 complement complex (host); NS-1  Infection (Streptococcus pneumonia): stratifin, cullin 1, selenoprotein K, metal response  element binding transcription factor 2, prostaglandin E synthase 2, HLA-B associated  transcript 4, zinc finger protein (C2H2 type) 276, GCIP-interacting protein p29, mitochondrial  ribosomal protein L20, aryl hydrocarbon receptor nuclear translocator-like, secretory carrier  membrane protein 1, nuclear receptor subfamily 5, group A, member 2, NIMA (never in  mitosis gene a)-related expressed, kinase 7, ribosomal protein L28, ribosomal protein S25,  lysosomal-associated protein transmembrane 5, neural precursor cell expressed,  developmentally, down-regulted gene 4, alpha glucosidase 2, alpha neutral subunit, coatomer  protein complex, subunit beta 2 (beta prime), ribosomal protein L3, NADH dehydrogenase  (ubiquinone) 1 alpha, subcomplex, assembly factor 1, isoprenylcysteine carboxyl  methyltransferase? cytoplasmic polyadenylation element binding protein 3, mannoside  acetylglucosaminyltransferase 1, RNA-binding region (RNP1, RRM) containing 1? folate  receptor 4 (delta), ATPase, H+ transporting, lysosomal 50/57 kDa, V1, subunit H, zinc finger,  DHHC domain containing 6, phosphoribosyl pyrophosphate synthetase-associated, protein 2,  choline/ethanolaminephosphotransferase 1? solute carrier family 38, member 1, ATP  synthase, H+ transporting, mitochondria! FO, complex, subunit f, isoform 2, glucose  phosphate isomerase 1, 2'-5'oligoadenylate synthetase 1A, tyrosine hydroxylase,  hemoglobin alpha, adult chain 1, selenoprotein P, plasma, 1, acetyl-Coenzyme A  dehydrogenase, long-chain, mannosidase, beta A, lysosomal? deltex 3 homolog  (Drosophila), ras homolog gene family, member AB, estrogen receptor 1 (alpha),  phosphoglycerate kinase 1, , keratin complex 2, basic, gene 8, emerin, nucleoporin 153,  formin 2, prothymosin alpha, synapsin l?+0cullin 4B, regulator of chromosome condensation  (RCC1) and, BTB (POZ) domain containing protein 1? immediate early response 5, SAM  domain and HD domain, 1, tumor rejection antigen gp96, lymphocyte antigen 6 complex,  locus E, , DAZ associated protein 2, general transcription factor II I, RNA polymerase II  transcriptional coactivator, SWI/SNF-related, matrix-associated actin-dependent, regulator of  chromatin, subfamily a, containing DEAD/H, box 1, structure specific recognition protein 1,  ankyrin repeat and FYVE domain containing 1, SET translocation, myocyte enhancer factor  2A, homeo box D9, H2A histone family, member Z, cellular nucleic acid binding protein?  golgi reassembly stacking protein 2, cathepsin L, eukaryotic translation initiation factor 5,  ubiquitin specific protease 9, X chromosome, proteasome (prosome, macropain) subunit,  alpha type 7, pescadillo homolog 1, containing BRCT domain, (zebrafish), heterogeneous  nuclear ribonucleoprotein K, DEAD (Asp-Glu-Ala-Asp) box polypeptide 52, sorting nexin 5,  cathepsin B, DnaJ (Hsp40) homolog, subfamily B, member 9, ribosomal protein S3a?  cytoplasmic polyadenylation element binding protein 4, 5'-3'exoribonuclease 2, small nuclear  ribonucleoprotein polypeptide F, , arachidonate 5-lipoxygenase activating protein, cytochrome  c oxidase, subunit Vic, RIKubiquinol cytochrome c reductase core protein 2, lactate  dehydrogenase 2, B chain, ubiquinol-cytochrome c reductase core protein 1, ATP synthase,  H+ transporting, mitochondria! FO, complex, subunit b, isoform 1, microsomal glutathione 5-  transferase 1, ras homolog gene family, member A, RAB7, member RAS oncogene family,  EGF-like module containing, mucin-like, hormone, receptor-like sequence 1, annexin A6,  mitogen activated protein kinase 3, tyrosine kinase, non-receptor, 2, villin 2, tubulin, beta 5,  catenin src (host); Pneumolysin, pneumococcal histidine triad D (PhtD), pneumococcal  histidine triad E (PhtE), LytB, and pneumococcal choline-binding protein A (PcpA)  Infection (Mycoplasma pneumonia): DnaK, L7/L12, P1, exotoxin  Infection (Campylobacterjejuni): gyrA, 16S rDNA, or flaA/flaB  Infection (Bacillus anthracis): Lethal factor, HtrA (BA3660), NIpC/P60-domain  endopeptidase (BA1952), BA0796 locus (BA0796), SAP  Infection (West Nile virus):  Infection (Human papilloma virus): E6, E7  Infection: RNase 7 (host) 

In some instances, the present method is used to inform the subject from whom the sample is derived about a health condition thereof. Health conditions that may be diagnosed or measured by the present method, device and system include, but are not limited to: chemical balance; nutritional health; exercise; fatigue; sleep; stress; prediabetes; allergies; aging; exposure to environmental toxins, pesticides, herbicides, synthetic hormone analogs; pregnancy; menopause; and andropause. The following Table B3 provides a list of biomarker that can be detected using the present invention, and their associated health conditions.

TABLE B3 Diagnostic Markers Health Condition Source Marker Diabetes Saliva pIgR, Arp 3, CA VI, and IL-1Ra; PLS-2, LEI, and IGJ chain, resistin miscellaneous ATP-binding cassette, sub-family C (CFTR/M RP), member 8; ATP- binding cassette, sub-family C (CFTR/MRP), member 9; angiotensin I converting enzyme (peptidyl-dipeptidase A) 1; adenylate cyclase activating polypeptide 1 (pituitary); adiponectin, C1Q and collagen domain containing; adiponectin receptor 1; adiponectin receptor 2; adrenomedullin; adrenergic, beta-2-, receptor, surface; advanced glycosylation end product-specific receptor; agouti related protein homolog (mouse); angiotensinogen (serpin peptidase inhibitor, clade A, member 8); angiotensin 11 receptor, type 1; angiotensin II receptor-associated protein; alpha-2-HS-glycoprotein; v-akt murine thymoma viral oncogene homolog 1; v-akt murine thymoma viral oncogene homolog 2; albumin; Alstrom syndrome 1; archidonate 12- lipoxygenase; ankyrin repeat domain 23; apelin, AGTRL 1 Ligand; apolipoprotein A-I; apolipoprotein A-II; apolipoprotein B (including Ag(x) antigen); apolipoprotein E; aryl hydrocarbon receptor nuclear translocator; Aryl hydrocarbon receptor nuclear translocator-like; arrestin, beta 1; arginine vasopressin (neurophysin II, antidiuretic hormone, Diabetes insipidus, neurohypophyseal); bombesin receptor subtype 3; betacellulin; benzodiazepine receptor (peripheral); complement component 3; complement component 4A (Rodgers blood group); complement component 4B (ChiIdo blood group); complement component 5; Calpain-10; cholecystokinin; cholecystokinin (CCK)-A receptor; chemokine (C-C motif) ligand 2; CD14 molecule; 0D163 molecule; 0D36 molecule (thrombospondin receptor); 0D38 molecule; CD3d molecule, delta (CD3-TCR complex); CD3g molecule, gamma (CD3-TCR complex); CD40 molecule, TNF receptor superfamily member 5; CD40 ligand (TNF superfamily, member 5, hyper-IgM syndrome); 0D68 molecule; cyclin-dependent kinase 5; complement factor D (adipsin); CASP8 and FADD-like apoptosis regulator; Clock homolog (mouse); chymase 1, mast cell; cannabinoid receptor 1 (brain); cannabinoid receptor 2 (macrophage); cortistatin; carnitine palmitoyltransferase I; carnitine palmitoyltransferase II; complement component (3b/4b) receptor 1; complement component (3d/Epstein Barr virus) receptor 2; CREB binding protein (Rubinstein-Taybi syndrome); C-reactive protein, pentraxin-related; CREB regulated transcription coactivator 2; colony stimulating factor 1 (macrophage); cathepsin B; cathepsin L; cytochrome P450, family 19, subfamily A, polypeptide 1; Dio-2, death inducer-obliterator 1; dipeptidyl-peptidase 4 (CD26, adenosine deaminase complexing protein 2); epidermal growth factor (beta- urogastrone); early growth response 1; epididymal sperm binding protein 1; ectonucleotide; pyrophosphatase/phosphodiesterase 1; ElA binding protein p300; coagulation factor XIII, Al polypeptide; coagulation factor VIII, procoagulant component (hemophilia A); fatty acid binding protein 4, adipocyte; Fas (TNF receptor superfamily, member 6); Fas ligand (TNF superfamily, member 6); free fatty acid receptor 1; fibrinogen alpha chain; forkhead box A2; forkhead box O1A; ferritin; glutamate decarboxylase 2; galanin; gastrin; glucagon; glucokinase; gamma-glutamyltransferase 1; growth hormone 1; ghrelin/obestatin preprohormone; gastric inhibitory polypeptide; gastric inhibitory polypeptide receptor; glucagon-like peptide 1 receptor; guanine nucleotide binding protein (G protein), beta polypeptide 3; glutamic-pyruvate transaminase (alanine aminotransferase); gastrin releasing peptide (bombesin); gelsolin (amyloidosis, Finnish type); hemoglobin; hemoglobin, beta; hypocretin (orexin); neuropeptide; precursor; hepatocyte growth factor (hepapoietin A; scatter factor); hepatocyte nuclear factor 4, alpha; haptoglobin; hydroxysteroid (11-beta); dehydrogenase 1; heat shock 70 kDa protein 1B; islet amyloid polypeptide; intercellular adhesion molecule 1 (CD54), human rhinovirus receptor; interferon, gamma; insulin-like growth factor 1 (somatomedin C); insulin-like growth factor 2 (somatomedin A); insulin-like growth factor binding protein 1; insulin-like growth factor binding protein 3; inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta; interleukin 10; interleukin 18 (interferon-gamma-inducing factor); interleukin 1, alpha; interleukin 1, beta; interleukin 1 receptor antagonist; interleukin 2; interleukin 6 (interferon, beta 2); interleukin 6 receptor; interleukin 8; inhibin, beta A (activin A, activin AB alpha polypeptide); insulin; insulin receptor; insulin promoter factor-1; insulin receptor substrate 1; insulin receptor substrate-2; potassium inwardly-rectifying channel, subfamily J, member 11; potassium inwardly-rectifying channel, subfamily J, member 8; klotho; kallikrein B, plasma (Fletcher factor) 1; leptin (obesity homolog, mouse); leptin receptor; legumain; lipoprotein, Lp(a); lipoprotein lipase; v-maf musculoaponeurotic brosarcoma oncogene homolog A (avian); mitogen-activated protein kinase 8; interacting protein 1; mannose- binding lectin (protein C) 2, soluble (opsonic defect); melanocortin 4 receptor; melanin-concentrating hormone receptor 1; matrix metallopeptidase 12 (macrophage elastase); matrix metallopeptidase 14 (membrane-inserted); matrix metallopeptidase 2 (gelatinase A, 72 kDa gelatinase, 72 kDa type IV collagenase); matrix metallopeptidase 9 (gelatinase B, 92 kDa gelatinase, 92 kDa type IV collagenase); nuclear receptor co-repressor 1; neurogenic differentiation 1; nuclear factor of kappa light polypeptide gene enhancer in B-cells 1(p105); nerve growth factor, beta polypeptide; non-insulin-dependent Diabetes Mellitus (common, type 2) 1; non- insulin-dependent Diabetes Mellitus (common, type 2) 2; Noninsulin- dependent Diabetes Mellitus 3; nischarin (imidazoline receptor); NF- kappaB repressing factor; neuronatin; nitric oxide synthase 2A; Niemann-Pick disease, type 02; natriuretic peptide precursor B; nuclear receptor subfamily 1, group D, member 1; nuclear respiratory factor 1; oxytocin, prepro-(neurophysin I); purinergic receptor P2Y, G-protein coupled, 10; purinergic receptor P2Y, G- protein coupled, 12; purinergic receptor P2Y, G-protein coupled, 2; progestagen-associated endometrial; protein (placental protein 14, pregnancy-associated endometrial alpha-2-globulin, alpha uterine protein); paired box gene 4; pre-B-cell colony enhancing factor 1; phosphoenolpyruvate carboxykinase 1 (PEPCK1); proprotein convertase; subtilisin/kexin type 1; placental growth factor, vascular; endothelial growth factor-related protein; phosphoinositide-3-kinase, catalytic, alpha polypeptide; phosphoinositide-3-kinase, regulatory subunit 1 (p85 alpha); phospholipase A2, group XI IA; phospholipase A2, group IID; plasminogen activator, tissue; patatin-like phospholipase domain containing 2; proopiomelanocortin (adrenocorticotropin/beta- lipotropin/alpha-melanocyte stimulating hormone/beta- melanocyte stimulating hormone/beta-endorphin); paraoxonase 1 ESA, PON, Paraoxonase; peroxisome proliferative activated receptor, alpha; peroxisome proliferative activated receptor, delta; peroxisome proliferative activated receptor, gamma; peroxisome proliferative activated receptor, gamma, coactivator 1; protein phosphatase 1, regulatory (inhibitor) subunit 3A (glycogen and sarcoplasmic reticulum binding subunit, skeletal muscle); protein phosphatase 2A, regulatory subunit B'(PR 53); protein kinase, AMP-activated, beta 1 non- catalytic subunit; protein kinase, cAMP-dependent, catalytic, alpha; protein kinase C, epsilon; proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 (Bridge-1); prostaglandin E synthase; prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase); protein tyrosine phosphatase, mitochondria! 1; Peptide YY retinol binding protein 4, plasma (RBP4); regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein); resistin; ribosomal protein S6 kinase, 90 kDa, polypeptide 1; Ras-related associated with Diabetes; serum amyloid Al; selectin E (endothelial adhesion molecule 1); serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6; serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1; serum/glucocorticoid regulated kinase; sex hormone-binding globulin; thioredoxin interacting protein; solute carrier family 2, member 10; solute carrier family 2, member 2; solute carrier family 2, member 4; solute carrier family 7 (cationic amino acid transporter, y+30 system), member 1(ERR); SNF1-like kinase 2; suppressor of cytokine signaling 3; v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog (avian); sterol regulatory element binding transcription factor 1; solute carrier family 2, member 4; somatostatin receptor 2; somatostatin receptor 5; transcription factor 1, hepatic; LF-B1, hepatic nuclear factor (HNF1); transcription factor 2, hepatic, LF-B3, variant hepatic nuclear factor; transcription factor 7-like 2 (T-cell specific, HMG-box); transforming growth factor, beta 1 (Camurati-Engelmann disease); transglutaminase 2 (C polypeptide, protein-glutamine-gamma- glutamyltransferase); thrombospondin 1; thrombospondin, type I, domain containing 1; tumor necrosis factor (TNF superfamily, member 2); tumor necrosis factor (TNF superfamily, member 2); tumor necrosis factor receptor superfamily, member 1A; tumor necrosis factor receptor superfamily, member 1B; tryptophan hydroxylase 2; thyrotropin-releasing hormone; transient receptor potential cation channel, subfamily V, member 1; thioredoxin interacting protein; thioredoxin reductase 2; urocortin 3 (stresscopin); uncoupling protein 2 (mitochondria!, proton carrier); upstream transcription factor 1; urotensin 2; vascular cell adhesion molecule 1; vascular endothelial growth factor; vimentin; vasoactive intestinal peptide; vasoactive intestinal peptide receptor 1; vasoactive intestinal peptide receptor 2; von VVillebrand factor; Wolfram syndrome 1 (wolframin); X-ray repair complementing defective repair in Chinese hamster cells 6; c-peptide; cortisol; vitamin D3; estrogen; estradiol; digitalis-like factor; oxyntomodulin; dehydroepiandrosterone sulfate (DHEAS); serotonin (5- hydroxytryptamine); anti-CD38 autoantibodies; gad65 autoantibody; Angiogenin, ribonuclease, RNase A family, 5; Hemoglobin A1c; Intercellular adhesion molecule 3 (CD50); interleukin 6 signal transducer (gp130, oncostatin M receptor); selectin P (granule embrane protein 140 kDa, antigen CD62); TIMP metallopeptidase inhibitor; Proinsulin; endoglin; interleukin 2 receptor, beta; insulin-like growth factor binding protein 2; insulin-like growth factor 1 receptor; fructosamine, N- acetyl-beta-d-glucosaminidase, pentosidine, advanced glycation end product, beta2-microglobulin, pyrraline Metabolic Serum GFAP autoantibodies syndrome/ prediabetes Kidney saliva Lactoferrin, uric acid, cortisol, alpha-amylase failure/ miscellaneous ADBP-26, NHE3, KIM-1, glutamyltransferase, N-acetyl-beta-D- disease glucosaminidase, lysozyme, NGAL, L-FABP, bikunin, urea, prostaglandins, creatinine, alpha-1-microglobulin, retinol binding protein, glutathione-S-transferases, adiponectin, beta-2- macroglobuin, calbindin-D, cysteine-rich angiogenic inducer 61, endothelial/epithial growth factors, alpha-1-acid glycoprotein (orosomucoid), prealbumin, modified albumin, albumin, transferrin, alpha-1-lipoprotein, alpha-1-antitrypsin matrix metalloproteinases (MMPs), alpha-1-fetoprotein, Tamm Horsfall protein, homoarginine, interleukin 18, monocyte chemotactic protein-1 (MCP-1), Lipocalin, VCAN, NRP1, CCL2, CCL19, COL3A1, GZMM, alpha- galactosidase, casein kinase 2, IP-10, Mig, I-TAC, MIP-1 a, MIP-3a, and MIP-113, alpha-2-glycoprotein-Zinc, leucine-rich alpha-2- glycoprotein, uromodulin, Pacsin 2, hepcidin-20, hepcidin-25, AIF-2, urinary type-IV collagen, lipocalin-type prostaglandin D synthase (L- PGDS), urinary neutrophil gelatinase-associated lipocalin (uNGAL), Annexin Al, Rab23, Shh, Ihh, Dhh, PTCH1, PTCH2, SMO, Gli1, Gli2, Gli3, TLR4, cystatin C, AQPI, AQP2, AQP3, NKCC2, NaPill, DAHKSEVAHRFKD [RNA:] SLC12A1, UMOD, vWF, MMPI, MMP3, SLC22A6, SLC22A 8, SLC22A 12, podocin, cubulin, LRP2, AQP9, and albumin, carcinoembryonic antigen (CEA), mucin, alpha-fetoprotein, tyrosinase, melanoma associated antigen, mutated tumor protein 53, p21, PUMA, prostate-specific antigen (PSA) or thyroglobulin, von VVillebrand factor (VWF), thrombin, factor VIII, plasmin, fibrin, osteopontin (SPP1), Rab23, Shh, Ihh, Dhh, PTCH1, PTCH2, SMO, Gli1, Gli2, Gli3 Liver miscellaneous Carnitine; Cholic Acid; Chenodeoxycholic, Deoxycholic, Lithocholic, failure/ Glycocholic; Prostaglandin E₂; 13,14-dihydro-15-keto Prostaglandin disease A2; Prostaglandin B2; Prostaglandin F2a; 15-keto-Prostaglandin F2α; 6-keto-Prostaglandin Fla; Thromboxane B2; 11-dehydro- Thromboxane B2; Prostaglandin D2; Prostaglandin J2; 15-deoxy-Al 2,14-Prostaglandin J2; 11β-Prostaglandin F2α; 5(S)- Hydroxyeicosatetraenoic acid; 5(S)-Hydroxyeicosapentaenoic acid; Leukotriene B4; Leukotriene B5; Leukotriene 04; Leukotriene D4; Leukotriene E4; Leukotriene F4; 12(S)-Hydroxyeicosatetraenoic acid; 12(S)-Hydroxyeicosapentaenoic acid; 15(S)- Hydroxyeicosatetraenoic acid; 15(S)-Hydroxyeicosapentaenoic acid; Lipoxin A4; 8(S)-Hydroxyeicosatetraenoic acid; 9- Hydroxyeicosatetraenoic acid; 11-Hydroxyeicosatetraenoic acid; 8- iso-Prostaglandin F2a; 9-Hydroxyoctadecadienoic acid; 13- Hydroxyoctadecadienoic acid; 20(S)-Hydroxyeicosatetraenoic acid; 9,10-Epoxyoctadecenoic acid; 12,13-Epoxyoctadecenoic acid; 12,13-Dihydroxyoctadecenoic acid; 5,6-Epoxyeicosatrienoic acid; 11,12-Epoxyeicosatrienoic acid; 14,15-Epoxyeicosatrienoic acid; 5,6-Dihydroxyeicosatrienoic acid; 8,9-Dihydroxyeicosatrienoic acid; 11,12-Dihydroxyeicosatrienoic acid; 14,15-Dihydroxyeicosatrienoic acid; 14,15-Epoxyeicosatetraenoic acid; 17,18- Epoxyeicosatetraenoic acid; 14,15-Dihydroxyeicosatetraenoic acid; 17,18-Dihydroxyeicosatetraenoic acid; 19,20- Dihydroxydocosapentaenoic acid; diacetylspermine, hemopexin, TLR4 Heart miscellaneous SFRP-3, NT-proBNP, troponin T, SKITHRIHWESASLL (SEQ ID NO: failure 6), AHKSEVAHRFK (SEQ ID NO: 7), uroguanylin, BNP Cardiovascular miscellaneous miR-378, miR-497, miR-21, miR-15b, miR-99a, miR 29a, miR-24, health miR-30b, miR-29c, miR-331.3p, miR-19a, miR-22, miR-126, let-7b, miR-502.3, and miR-652 IL-16, sFas, Fas ligand, MCP-3, HGF, CTACK, EOTAXIN, adiponectin, IL-18, TIMP.4, TIMP.1, CRP, VEGF, and EGF saliva C-reactive protein (CRP); myoglobin (MYO), creatinine kinase myocardial band (CK-MB), cardiac troponins (cTn), and myeloperoxidase; TNF-α, and MMP-9; CD40 High saliva lysozyme blood pressure Tiredness/ urine endorepellin fatigue saliva PPGKPQGPPPQGGNQPQGPPPPPGKPQ (SEQ ID NO: 1); GNPQGPSPQGGNKPQGPPPPPGKPQ (SEQ ID NO: 2); SPPGKPQGPPQQEGNKPQGPPPPGKPQ (SEQ ID NO: 3) urine human herpesvirus 6, human herpesvirus 7, human cytomegalovirus, and Epstein-Barr virus (EBV) miscellaneous GGHPPPP (SEQ ID NO: 4), ESPSLIA (SEQ ID NO: 5); Malnutrition Saliva sIgA Depressive miscellaneous Secretogranin, VGF disorder Alzheimer's CSF, β-amyloid(1-42), β-amyloid(1-40), tau, phosphor-tau-181 disease serum, saliva Stress saliva Cortisol, dehydro-androsteronesulfate; 17-ketosteroidsulfate; dehydro-epiandrostronesulfate; corticosteroid, 17- hydroxycorticosteroid, chromogranin A, alpha-amylase, secretary IgA, lysozyme, growth hormone, oxytocin miscellaneous aldose reductase, apoptosis signal-regulating kinase 1, aquaporin 5, beta-endorphin, betaine GABA transporter, caspase recruitment domain protein 9, caspase 8, cyclin D, cyclooxygenase 2, cytochrome P450, cytochrome c, c-fos, c-jun, epidermal growth factor receptor, ferritin, glucocorticoid receptor, glucose regulated protein 58, glucose regulated protein 75, glutathione 5-transferase p, GroEL, heat shock protein 25/27, heat shock protein 40, heat shock protein 60, heat shock protein 70, heat shock protein 90, heat shock transcription factor-1, heme oxygenase-1, interleukin 113, interleukin 6, interleukin 8, interleukin 10, interleukin 12, laminin, leptin receptor, matrix metalloproteinase 9, metallothionein, Mek-1, Mekk-1, inducible nitric oxide synthase, peripheral benzodiazepine receptor, p38 MAPK, salivary alpha amylase, SAPK, serotonin, serotonin receptor, substance P, superoxide dismutase Mn, superoxide dismutase Cu/Zn, superoxide dismutase EC, transforming growth factor β, tumor suppressor p53, and vasoactive intestinal peptide Circadian saliva melatonin rhythm Bone Urine Pyridinoline, deoxypyridinoline, collagen type 1 corss-linked N- turnover/ telopeptide (NTX), collagen type 1 corss-linked C-telopeptide (CTX), Osteoporosis bone sialoprotein (BSP), Tartrate-resistant acid phosphatase 5b saliva deoxypyridinium (D-PYR) and osteocalcin (OC), hepatocyte growth factor and interleukin-1 beta Muscle Serum, Myoglobin, creatine kinase (CK), lactate dehydrogenase (LDH), damage urine aldolase, troponin, carbonic anhydrase type 3 and fatty acid-binding protein (FABP), transaminases Exercise/ sweat urea athletic serum Myostatin, follistatin-like related gene activity saliva testosterone Performance miscellaneous interleukin-6, interleukin-1 beta, G-CSF, interferon-gamma, enhancement interleukin-8, interleukin-9, MCP-1, MIP-beta, and/or TNF alpha Energy Serum AMPK balance Urine, pre-albumin, retinol binding protein, urea (protein sweat, excretion)/ feces energy miscellaneous cholesterol, lipoproteins, insulin, insulin C peptide, IGF binding status/ proteins, e.g. IGF-BPI, liver enzymes metabolic state Growth Saliva IGF-1 Andropause saliva testosterone; testosterone precursors such as pregnenolone, progesterone, 17-hydroxypregnenolone, 17-hydroxyprogesterone, dehydroepiandrosterone (DHEA) and delta-4-androstene-3,17- dione; testosterone and dihydrotestosterone metabolites such as the 17-ketosteroids androsterone and etiocholanolone, polar metabolites in the form of diols, triols, and conjugates, as well estradiol, estrogens, androsteindione, cortisol, DHEA, FSH (follicle stimulating hormone), LH (luteinizing hormone), and GnRH (gonadotropin- releasing hormone) Menopause Saliva Follicle stimulating hormone (FSH) Estrogen and progesterone, testosterone, free testosterone, and dehydroepiandrosterone sulfate (DHEAS), cortisol and dehydro- epiandrosterone (DHEA) Pregnancy/ Saliva progesterone fetal urine human chorionic gonadotropin, Levonorgestrel, alpha-fetoprotein development serum estradiol Breast urine 47D10 antigen, PTCD2, 5L025A20, NFKB2, RASGRP2, PDE7A, cancer MLL, PRKCE, GPATC3, PRI0285 and GSTA4, MIPEP, PLCB2, SLC25A19, DEF6, ZNF236, C18orf22, COX7A2, DDX11, TOP3A, C9orf6, UFC1, PFDN2, KLRD1, LOC643641, HSP90AB1, CLCN7, TNFAIP2, PRKCE, MRPL40, FBF1, ANKRD44, CCT5, USP40, UBXD4, LRCH1, MRPL4, SCCPDH, STX6, LOC284184, F1123235, GPATC3, CPSF4, CREM, HIST1H1D, HPS4, FN3KRP, ANKRD16, 08 orf16, ATF71P2, PRI0285 Prostate Serum/ Prostate specific antigen (PSA) cancer saliva Urine PCA3, GOLPH2, SPINK1, TMPRSS2:ERG Infections See Table B2 Dental Saliva aspartate aminotransferase (AST) and alkaline phosphatase (ALP), caries/ uric acid and albumin; 12-HETE; MMP-8, TIMP-1, and ICTP periodontal disease Heavy saliva lead, cadmium metal poisoning Drugs/ saliva marijuana, Cocaine (crystalline tropane alkaloid), methamphetamine, drug amphetamine, heroin, methyltestosterone, mesterolone, morphine, metabolites cyclophosphamide metabolites, Haloperidol, barbiturates; antipyrine, caffeine, cisplatin, cyclosporine, diazepam, digoxin, methadone, phenytoin, theophylline, tolbutamide. Nicotine/cotinine, cannabis urine trichloroethanol glucuronide, Anabolic steroids, Androstenedione, Benzodiazepines, Chlordiazepoxide, Lorazepam, Zidovudine Allergies saliva Allergen-specific IgAs (see Tables B7 and 9)

In some instances, the biomarker that can be detected by the present method is an antibody in a sample, e.g., a diagnostic sample, that is probative for diagnosing a disease or health condition of the subject from which the sample is derived.

Tables B4 provides a list of autoantibody targets, which can be used, in whole or as an epitope fragment, as a capture agent in the present method to measure the amount of the epitope-binding antibody analyte in a sample and thereby diagnose the associated disease or health condition, e.g., an autoimmune disease. In some cases, the disease or health condition is related to an immune response to an allergen. Table B5 provides a list of allergens, which can be used, in whole or as an epitope fragment, as a capture agent in the present method to measure the amount of the epitope-binding antibody analyte in a sample and thereby diagnose the associated disease or health condition, e.g., an allergy. In certain instances, the disease or health condition is related to an infectious disease, where the infectious agent may be diagnosed based on information including the measured amount of antibodies against one or more epitopes derived from the infectious agent (e.g., lipopolysaccharides, toxins, proteins, etc.). Tables B6 provides a list of infectious-agent derived epitopes which can be used, in whole or as an epitope fragment, as a capture agent in the present method to measure the amount of the epitope-binding antibody analyte in a sample and thereby diagnose the associated disease or health condition, e.g., an infection. Other epitopes or antigens that may be suitable for use in the present diagnostic method are described in, e.g., PCT App. Pub. No. WO 2013164476, which is incorporated herein by reference.

TABLE B4 Diagnostic Autoantibody Epitopes Disease/condition Autoantibody Targets Cancer ACAA2; ANXA13; AQP2; ASPA; BCL2; BCL2L1; BIK; CD160; CD37; CDK4; CDK6; CHEK2; CITED2; CNN2; CTSC; CTSZ; CycE2; ELK1; FGF10; FN1; GATA3; GJA1; GNRH1; GRB2, HBB; HBE1; HIST2H2AA; HPRT1; ID2; IER2; IFI27; IFITM1; IFITM2; IL15; IL18; IL8; IL9; KRT16; LALBA; LDHA; LDHB; LECT1; MAFK; Mage3; MAGEA3; MMP2; NPPB; OAS1, p21; p53; PCNA; PENK; PEX3; PHB; PHYH; PI3; PKBα; PLN; S100A7; SCAMP1; SCGB1A1; SLC38A5; SNRP2; SNX9; SST; SSTR2; TACSTD1; TNNC2; TOB1; TSG101; VDRIP; WNT2, p62 and Koc; ZFP161, Ubiquilin-1, HOX- B6, YB-1, Osteonectin, ILF3 Squamous cell protein kinase C and p53-binding protein (TP53 BP), lymphoid blast crisis lung carcinoma oncogene (LBC), Small cell lung SOX families B1 and B2, MUC-1, cancer Lung cancer MUC-1, p53, surviving, LAMR1, annexin I, 14-3-3-theta; AKR1B10; GOT2; HNRPR; PDIA3; NME2; RTN4; HI1FX; G3BP; HSPCA; ACTN4; PGP9. 5; Colorectal cancer MUC-1, surviving, p-53; translationally controlled tumor protein; HSPC218; Ribosomal protein S18; v-Fte-1; v-Fos transformation effector protein; MAGEA3, SSX2, NY-ESO-1, HDAC5, MBD2, TRIP4, NY-CO-45, KNSL6, HIP1R, Seb4D, KIAA1416, and LMNA; UCHL3 Hepatocellular fibrillarin and p330d/CENP-F, insulin-like growth factor II mRNA-binding carcinoma proteins (IMP) 1, IMP3 and p53, NOR-90, nucleophosmin/protein B23, cyclin B1, DNA topoisomerase II (topo II), p62, HCC1, SG2NA, MAGE-C2, AF146731; AF219119; AF146019; Ligatin; AF220416; AF218421; AF257175; AF244135; AF243495; AF287265; AF258340; AF270491; AF286340; small nuclear RNA-associated sm-like protein; Dna J protein; CENP-F; translationally controlled tumor protein; LDH-A; Albumin; Hsp89αΔN; SEC63; AF100141; 14, 5 kDa protein; GCF2; Metallopanstimulin 1; SMP-30 D31815; Cg1 protein,; C3VS protein; F1-ATPase, β subunit; Human ribosomal protein L10; Pre-apolipoprotein CIII; Galactose-1- phosphate-uridyl-transferase (GALT); DNA polymerase Δ, small subunit; Mitochondrial DNA Renal cancer AF257175; small nuclear RNA-associated sm-like protein; Dna J protein; smooth muscle protein 22-alpha (SM22-alpha); carbonic anhydrase I (CAI) Acute leukemia Rho GDP dissociation inhibitor 2, γ-actin, F-actin capping protein (CAPZA1), heterogeneous nuclear ribonucleoprotein L (hnRNP L), tubulin-α 6, PCNA Chronic KIAA1641; PIPMT; FosB; ZNF268; SEBD4; Ikaros; p75/LDEGF; CHIP; lymphocytic PYGB; ZNF148; KIAA0336; RPL11; FMNL; HGRG8 leukemia non-Hodgkin's CENP-F, lymphoma Multiple myeloma NY-ESO-1 melanoma NY-ESO-1, MAGE-1, BAGE, GAGE, MART-1/melan A, gp100, and tyrosinase Pancreatic Calreticulin, DEAD-box protein 48 (DDX48) cancer Ovarian cancer ACSBG1, AFP, CSNK1A1 L, DHFR, MBNL1, TP53, PRL, PSMC1, PTGFR, PTPRA, RAB7L1, and SCYL3, her2/neu, MUC1, c-myc, ECPKA, and NY-ESO-1, p53, UBQLN1, HOXB6, TOP2A, putative helicase-RUVBL (RUVBL), HMBA-inducible (HEXIM1), DDX5 and HDCMA Prostate cancer Bcl2, NY-ESO-1, survival protein lens epithelium-derived growth factor p75 (LEDGF/p75), PRDX6/AOP2, clusterin, DJ-1, superoxide dismutase, alcohol dehydrogenase, HSP70, HSP27/HSPB1, lactoylglutathione lyase, glucose- regulated protein-78 kDa (GRP78), p62, Koc, and IMP1, α-Methylacyl- coenzyme A racemase and 5-α-reductase, AKRIA1; Brd2; C17 orf 25; CAPZA1; c-MYC; Cyclin A; Cyclin B1; Cyclin D1; Drebrin; eIF4G1; HIP1; HSPA8; Lactoylglutathione lyase; MAD-CT-1; MAD-CT-2; No55; P53; P62; P90; PP4R; PIP; PSA; RPL13a; RPL22; Survivin; Syntenin 1; TDP-43; VCP; vWF; Lage-1, and Xage-1; bromo domain-containing protein 2 (BRD2), ribosomal proteins L22 and L13a, XP_373908 Breast cancer p53, c-myc, NY-ESO-1, BRCA1, BRCA2, HER2, MUC1, IGFBP-2, TOPO2α, ribosomal protein S6, eukaryotic elongation factor 2, eukaryotic elongation factor 2 kinase, and heat shock protein 90 (HSP90), Ku protein, topoisomerase I, and the 32-kDa subunit of replication protein A; CENP-F; AF146731; int-2, pentraxin I, integrin beta5, cathepsin L2 and S3 ribosomal protein; RNA-binding protein regulatory subunit (RS), DJ-1 oncogene, glucose-6-phosphate dehydrogenase, heat shock 70-kDa protein 1 (HS71), and dihydrolipoamide dehydrogenase Nasopharyngeal MAGE, HSP70, Fibronectin, CD44, EBV antigens carcinoma Oral cancer Cyclin B1, p53 Oral squamous p53 cell carcinoma Head and neck CASP-8, SART-1, TREX1, 3′ repair exonuclease; BRAP (BRCA1 squamous cell associated): Nuclear localization protein; Trim 26 zinc finger domains; carcinoma GTF21 transcription factor. Murine homolog TF11-1; NSEP1 (YB-1) transcription factor; MAZ transcription factor associated with c-myc; SON (DBP-5; KIAA1019; NREBP DNA binding protein); NACA nascent polypeptide-associated complex; NUBP2 nucleotide binding protein; EEF2 Translation elongation factor 2; GU2 Putative RNA helicase; RPLI3A ribosomal protein; SFRS21P (CASP11; SIP1; SRRP1290 splicing factor); RPS12 ribosomal protein; MGC2835 RNA helicase; TMF1, TATA modulatory factor; PRC1 regulator of cytokinesis; KRT14 keratin 14; Viniculin; H2AFY histone family member; SLK (KIAA02304) Ste related kinase; NOL3 (ARC) nuclear protein 3, apoptosis repressor; DNAJA2 member of Hsp40 family; DNAJA1 member of HSP40 family; LINE-1 retrotransposon; MOG (HSPC 165) Homolog of yeast protein; LIMS1 (PINCH): LIM and senescent antigen-like domain; COPB2 coatomer protein complex subunit protein; FLJ22548 hypothetical protein; C21orf97; FLJ21324; MGC15873; SSNA1 Sjogrens syndrome nuclear autoantigen 1; KIAA0530, zinc finger domain; rat stannin; hypothetical protein DKFZp4340032; human FLJ23089; PC326 Esophageal NY-ESO-1; SURF1, HOOK2, CENP-F, ZIC2, hCLA-iso, Ki-1/57, enigma, cancer HCA25a, SPK, LOC146223 and AGENCOURT_7565913 Metabolic GFAP syndrome/ prediabetes Diabetes Zn transporter 8, glutamic acid decarboxylase (GAD), CD38, gad65, IA2, insulin, MRPS31, ICA1, L-type voltage gated calcium channel; SNRPB2; DDX42; C11orf63; TCOF1; TSSK2; KDM4B; PDGFB; LTK; RPL14; VIM; GTF2I; BCL2L13; LARP6; DKFZP434K028; USP39; SERBP1; CCL19; GAD2; MCM10; ZNF688; PTEN; RP6-166C19.11; GIPC1; TIGD1; CCDC131; HTF9C; SOX5; MCF2L; TRAF3IP1; 6CKINE; ACY3; AMMECR1L; ARHGAP9; ASNS; BATF2; BMX; C9ORF25; CDC2; CHGB; CXORF38; CXORF56; DMD; ECHDC1; EIF3F; EPHA2; ERMN; FAM136A; (includes; EG: 84908); FILIP1; FLT1; GART; GIMAP6; GNG7; GTF2F1; HGS; IFI6; KDM4B; LACE1; LGALS1; LGALS7; LIMS2; LTK; LUC7L; NCAPG; (includes; EG: 64151); NME6; NUPL1; PAK4; PDE4DIP; PSIP1; RAB20; RNGTT; RPS3; SPG20; TALDO1; TBRG1; THAP1; TRAF3IP2; UBL4A; ZC3HC1; ZNF131; RAD51AP1; HADH; (HADH); C11orf16; (C11orf16); TAC3; ABR; ECE1; PPP1R2; GRINL1A; ABR; C19orf44; MUSTN1; ETHE1; BMI1; BAZ2B; ; TBC1D22A; CAMK2N2; ASS1; CCNY; MARK2; RAD51AP1; RAB38; RIOK1; HSP90AA1; C11orf74; ARID3A; LMOD1; CAPRIN1; ITGB3BP; MND1; SGK; NADK; MED9; LDHA; ARHGAP26; ANKRA2; CRY2; IL23A; DUSP14; ZBTB44; SIRT1; SLC2A3; GPR172B; CCDC89; BATF; HMOX1; ARRDC1; USF2; GBGT1; EDC3; SGIP1; GCGR; ZRANB2; NLGN4Y; GJB6; CDK10; PSG1; CCDC74A; DENND1C; MAP2K6 Autoimmune cardiac troponin I (cTnl) heart disease Immunoglobulin PRKD1, MATN2, DDX17, UBE2W, CDKN1 B, SOD2, FLOT2, IQCK, A nephropathy BLZF1, BRD9, CDS2, EFNA3, EIF4A2, FLU, LIMCH1, MAGEA4, MEF2D, MLLT6, MRPL28, MUTED, NKAIN4, PCTK1, PLXNA1, PODN, POLH, PRKD2, RNF1 1 3A, SEPT5, TNS1, TOM1, TRPV4, USP12, ZMYM3, CIAPIN1, GDI2, HSPA8, SERPINA5 and TGM1 End stage renal IGLC1; IGHG1; EDC3; IGHG1; APEX2; CD3D; TRIM21; IGKV1-5; IGHG3; disease CTLA-FC; CD7; CLIP4; MAPRE1; SNRPB2; IGHG1; ZBTB44; CD3D; IGHG1; TRAM1; ERR beta-; LBD; CNBP; OLFM1; IGHM; SIRT5; CEP290; PHLDA1 Glomerular nephritis Addison's 21-hydroxylase, P450-17α-hydroxylase (17OH) and P450-side chain disease cleavage (SCC) Primary ovarian Jo-1, proteinase 3 (PR3) insufficiency Sjögren's IgA, IgG, IgM autoantibodies; IgA, lactoferrin and beta2-microglobulin; syndrome lysozyme C, and cystatin C, amylase and carbonic anhydrase SSA/Ro; LA/SS-B Systemic lupus CDC25B, APOBEC3G, ARAF, BCL2A1, CLK1, CREB1, CSNK1G1, erythematosus CSNK2A1, CWC27, DLX4, DPPA2, EFHD2, EGR2, ERCC2, EWSR1, (SLE) EZH2, FES, FOS, FTHL17, GEM, GNA15, GNG4, HMGB2, HNRNPUL1, HOXB6, ID2, IFI35, IGF2BP3, IGHG1, JUNB, KLF6, LGALS7, LIN28A, MLLT3, NFIL3, NRBF2, PABPC1, PATZ1, PCGF2, PPP2CB, PPP3CC, PRM1, PTK2, PTPN4, PYGB, RET, RPL18A, RPS7, RRAS, SCEL, SH2B1, SMAD2, STAM, TAF9, TIE1, UBA3, VAV1, WT1, ZAP70, orZNRDI KIT, C6orf93, RPL34, DOM3Z, COPG2, DNCL12, RRP41; FBXO9; RALBP1, PIAS2; EEF1D; CONI; KATNB1; POLR2E; CCT3; KIAA0643; RPL37A, GTF2H2; MAP2K5; CDK3; RPS6KA1; MARK4, MTO1; MGC42105; NFE2L2; WDR45L, STK4, PFKFB3; NTRK3; MLF1; TRIM37, ACTL7B, RPL18A, CKS1B; TUBA1, NME6, SUCLA2, IGHG1, PRKCBP1; BAG3; TCEB3; RPL15, SSX4; MAP2K7; EEF1G; RNF38, PHLDA2, KCMF1; NUBP2, VPS45A SSA/Ro; dsDNA; Smith; histones; thrombin; v-Fos transformation effector protein, tryptase, Sm antigen, beta 2; cardiolipin; glycoprotein I β2; Endothelial PC/activated PC receptor; human gamma enolase CREST centromere syndrome Systemic Type I topoisomerase sclerosis Primary biliary nucleoporin 62, Sp100 nuclear antigen, nucleoporin 210 kDa, mitochondria, cirrhosis mitochondrial pyruvate dehydrogenase (PDH) or E3 binding protein Dermatitis eTG herpetiformis Miller-Fisher ganglioside GQ1B Syndrome Wegener's c-ANCA granulomatosis Neuropathies ganglioside GD3, ganglioside GM1, GA1, GM2, MAG microscopic p-ANCA polyangiitis Polymyositis Signal recognition particles scleromyositis exosome complex Signal recognition particles myasthenia nicotinic acetylcholine receptor Signal recognition particles, muscle-specific gravis kinase (MUSK) Signal recognition particles Lambert-Eaton voltage-gated calcium channel (P/Q-type) myasthenic syndrome Hashimoto's thyroid peroxidase thyroiditis Graves' disease TSH receptor paraneoplastic Hu, Yo (cerebellar Purkinje Cells), amphiphysin cerebellar syndrome encephalitis voltage-gated potassium channel (VGKC), N-methyl-D-aspartate receptor (NMDA) Sydenham's basal ganglia neurons chorea antiphospholipid glycoprotein 1 (2GPI), Endothelial PC/activated PC receptor syndrome Systemic proteinase 3 (PR3) and myeloperoxidase (MPO) vasculitis Neuromyelitis aquaporin-4 Allergies Allergen-specific IgAs Rheumatoid Rheumatoid factor, cyclic citrullinated protein; human cartilage gp39 arthritis peptides and type II collagen; citrullinated fibrinogen, citrullinated vimentin, citrulline-substituted filaggrin peptides, hnRNP-A2/B1, BiP, tryptase Asthma tryptase Multiple sclerosis myelin basic protein, spectrin, fodrin, myelin oligodentrocyte glycoprotein, proteolipid protein (PLP), 2′,3′-cyclic nucleotide-phosphodiesterase (CNP), Glc(α1,4)Glc(α) (GAGA4), Glc(α1,6)Glc(α) (GAGA6) amyotrophic HMGB1 lateral sclerosis (ALS) Idiopathic platelet glycoprotein (GP) IIb/IIIa, GPIb/IX, GPIa/IIa thrombocytopenic purpura Thrombosis thrombomodulin Cardiovascular Endothelial PC/activated PC receptor; IL-1 alpha, alpha-actinin-2 (aActn2); disease alpha-Myosin Heavy Chain (alpha-MHC-S 1); SI fragment of alpha-Myosin Heavy Chain 6 (alpha-MHC6-SI); alpha-Myosin Heavy Chain 7 (MyHC7) post- ELAVL2, ELAVL3, ELAVL4, Nova-1, Nova-2, Cdr1, Cdr2; and Cdr3 streptococcal disease such as PANDAS, post- GABHS glomerulonephritis, rheumatic fever, autism and Syndenham's chorea Parkinson's alpha-synuclein; myelin basic protein (MBP), proteolipid protein (PLP), Disease myelin oligodendrocyte glycoprotein (MOG), myelin associated glycoprotein (MAG), oligodendrocytes specific protein (OSP) pernicious Vitamin B₁₂ anemia

TABLE B5 Allergen Epitopes Source Allergen mites Acas13, Blot1, Blot3, Blot4, Blot5, Blot6, Blot10, Blot11, Blot12, Blot13, Blot19; American house dust mite (Derf1, Derf2, Derf3, Derf7, Derf10, Derf11, Derf14, Derf15, Derf16, Derf17, Derf18w); house dust mite (Derm1); European house dust mite (Derp1, Derp2, Derp3, Derp4, Derp5, Derp6, Derp7, Derp8, Derp9, Derp10, Derp11, Derp14, Derp20, Derp21); mite (Eurm2; Eurm14); storage mite (Glyd2, Lepd2, Lepd5, Lepd7, Lepd10, Lepd13, Tyrp2, Tyrp13); Dermatophagoides farinae (Derf1.0101, Derf1.0102, Derf1.0103, Derf1.0104, Derf1.0105, Derf2.0101, Derf2.0102, Derf2.0103, Derf2.0104, Derf2.0105, Derf2.0106, Derf2.0107, Derf2.0108, Derf2.0109, Derf2.0110, Derf2.0111, Derf2.0112, Derf2.0113, Derf2.0114, Derf2.0115, Derf2.0116, Derf2.0117); Dermatophagoides pteronyssinus (Derp1.0101, Derp1.0102, Derp1.0103, Derp1.0104, Derp1.0105, Derp1.0106, Derp1.0107, Derp1.0108, Derp1.0109, Derp1.0110, Derp1.0111, Derp1.0112, Derp1.0113, Derp1.0114, Derp1.0115, Derp1.0116, Derp1.0117, Derp1.0118, Derp1.0119, Derp1.0120, Derp1.0121, Derp1.0122, Derp1.0123, Derp2.0101, Derp2.0102, Derp2.0103, Derp2.0104, Derp2.0105, Derp2.0106, Derp2.0107, Derp2.0108, Derp2.0109, Derp2.0110, Derp2.0111, Derp2.0112, Derp2.0113); Euroglyphus maynei (Eurm2.0101, Eurm2.0102); Glycyphagus domesticus (Glyd2.0101, Glyd2.0201); and Lepidoglyphus destructor (Lepd2.0101, Lepd2.0101, Lepd2.0101, Lepd2.0102, Lepd2.0201, Lepd2.0202) Pollen Short Ragweed (Ambrosia artemisiifolia) allergen, Amb a 1, Amba2, Amba3, Amba5, Amba6, Amba7, Amba8, Amba9, Amba10; Betula verrucosa allergen, Bet v 1, Phleum pratense allergen, Phl p 5), giant ragweed (Ambt5); mugwort (Artv1, Artv2, Artv3, Artv4, Artv5, Artv6); sunflower (Hela1, Hela2, Hela3); Mercurialis annua (Mera1); lamb's-quarters, pigweed (Chea1); white goosefoot (Chea2, Chea3); Russian-thistle (Salk1); Rosy periwinkle (Catr1); English plantain (Plal1); Japanese hop (Humj1); Parietaria judaica (Parj1, Parj2, Parj3); Parietaria officinalis (Paro1); Ambrosia artemisiifolia (Amba8.0101, Amba8.0102, Amba9.0101, Amba9.0102); Plantago lanceolata (Plal1.0101, Plal1.0102, Plal1.0103); and Parietaria judaica (Parj1.0101, Parj1.0102, Parj1.0201, Par2.0101, Parj2.0102, Parj3.0101, Parj3.0102), Bermuda grass (Cynd1, Cynd7, Cynd12, Cynd15, Cynd22w, Cynd23, Cynd24); orchard grass (Dacg1, Dacg2, Dacg3, Dacg5); meadow fescue (Fesp4w); velvet grass (Holl1); rye grass (Lolp1, Lolp2, Lolp3, Lolp5, Lolp11); canary grass (Phaa1); Timothy (Phlp1, Phlp2, Phlp4, Phlp5, Phlp6, Phlp11, Phlp12, Phlp13); Kentucky blue grass (Poap1, Poap5); Johnson grass (Sorh1); Cynodon dactylon (Cynd1.0101, Cynd1.0102, Cynd1.0103, Cynd1.0104, Cynd1.0105, Cynd1.0106, Cynd1.0107, Cynd1.0201, Cynd1.0202, Cynd1.0203, Cynd1.0204); Holcus lanatus (Holl1.0101, Holl1.0102); Lolium perenne (Lolp1.0101, Lolp1.0102, Lolp1.0103, Lolp5.0101, Lolp5.0102); Phleum pretense (Phlp1.0101, Phlp1.0102, Phlp4.0101, Phlp4.0201, Phlp5.0101, Phlp5.0102, Phlp5.0103, Phlp5.0104, Phlp5.0105, Phlp5.0106, Phlp5.0107, Phlp5.0108, Phlp5.0201, Phlp5.0202); and Secale cereale (Secc20.0101, Secc20.0201), Alder (Alng1); Birch (Betv1, Betv2, Betv3, Betv4, Betv6, Betv7); hornbeam (Carb1); chestnut (Cass1, Cass5, Cass8); hazel (Cora1, Cora2, Cora8, Cora9, Cora10, Cora11); White oak (Quea1); Ash (Frae1); privet (Ligv1); olive (Olee1, Olee2, Olee3, Olee4, Olee5, Olee6, Olee7, Olee8, Olee9, Olee10); Lilac (Syrv1); Sugi (Cryj1, Cryj2); cypress (Cupa1); common cypress (Cups1, Cups3w); mountain cedar (Juna1, Juna2, Juna3); prickly juniper (Juno4); mountain cedar (Juns1); eastern red cedar (Junv1); London plane tree (Plaa1, Plaa2, Plaa3); date palm (Phod2); Betula verrucosa (Betv1.0101, Betv1.0102, Betv1.0103, Betv1.0201, Betv1.0301, Betv1.0401, Betv1.0402, Betv1.0501, Betv1.0601, Betv1.0602, Betv1.0701, Betv1.0801, Betv1.0901, Betv1.1001, Betv1.1101, Betv1.1201, Betv1.1301, Betv1.1401, Betv1.1402, Betv1.1501, Betv1.1502, Betv1.1601, Betv1.1701, Betv1.1801, Betv1.1901, Betv1.2001, Betv1.2101, Betv1.2201, Betv1.2301, Betv1.2401, Betv1.2501, Betv1.2601, Betv1.2701, Betv1.2801, Betv1.2901, Betv1.3001, Betv1.3101, Betv6.0101, Betv6.0102); Carpinus betulus (Carb1.0101, Carb1.0102, Carb1.0103, Carb1.0104, Carb1.0105, Carb1.0106, Carb1.0106, Carb1.0106, Carb1.0106, Carb1.0107, Carb1.0107, Carb1.0108, Carb1.0201, Carb1.0301, Carb1.0302); Corylus avellana (Cora1.0101, Cora1.0102, Cora1.0103, Cora1.0104, Cora1.0201, Cora1.0301, Cora1.0401, Cora1.0402, Cora1.0403, Cora1.0404); Ligustrum vulgare (Ligv1.0101, Ligv1.01.02); Olea europea (Olee1.0101, Olee1.0102, Olee1.0103, Olee1.0104, Olee1.0105, Olee1.0106, Olee1.0107); Syringa vulgaris (Syrv1.0101, Syrv1.0102, Syrv1.0103); Cryptomeria japonica (Cryj2.0101, Cryj2.0102); and Cupressus sempervirens (Cups1.0101, Cups1.0102, Cups1.0103, Cups1.0104, Cups1.0105) mold Alternaria alternata allergen, Alt a 1, Alta3, Alta4, Alta5, Alta6, Alta7, Alta8, Alta10, Alta12, Alta13, Aspergillus fumigatus allergen, Asp f 1, Aspf2, Aspf3, Aspf4, Aspf5, Aspf6, Aspf7, Aspf8, Aspf9, Aspf10, Aspf11, Aspf12, Aspf13, Aspf15, Aspf16, Aspf17, Aspf18, Aspf22w, Aspf23, Aspf27, Aspf28, Aspf29); Aspergillus niger (Aspn14, Aspn18, Aspn25); Aspergillus oryzae (Aspo13, Aspo21); Penicillium brevicompactum (Penb13, Penb26); Penicillium chrysogenum (Pench13, Pench18, Pench20); Penicillium citrinum (Penc3, Penc13, Penc19, Penc22w, Penc24); Penicillium oxalicum (Peno18); Fusarium culmorum (Fuse1, Fusc2); Trichophyton rubrum (Trir2, Trir4); Trichophyton tonsurans (Trit1, Trit4); Candida albicans (Canda1, Canda3); Candida boidinii (Candb2); Psilocybe cubensis (Psic1, Psic2); shaggy cap (Copd, Copc2, Copc3, Copc5, Copc7); Rhodotorula mucilaginosa (Rhom1, Rhom2); Malassezia furfur (Malaf2, Malaf3, Malaf4); Malassezia sympodialis (Malas1, Malas5, Malas6, Malas7, Malas8, Malas9, Malas10, Malas11, Malas12, Malas13); Epicoccum purpurascens (Epip1); and Alternaria alternate (Alta1.0101, Alta1.0102), Aspergillus versicolor antigen, S. chartarum antigen), Cladosporium herbarum (Clah2, Clah5, Clah6, Clah7, Clah8, Clah9, Clah10, Clah12); Aspergillus flavus (Aspf113); mammals Bos domesticus dander allergen, Bos d 2, Bosd3, Bosd4, Bosd5, Bosd6, Bosd7, Bosd8, Bosd2.0101, Bosd2.0102, Bosd2.0103, Canis familiaris allergen, Can f 1, Canf2, Canf3, Canf4, Equus caballus allergen, Equc1, Equc2, Equc3, Equc4, Equc5, Felis domesticus allergen, Fel d 1, Feld2, Feld3, Feld4, Feld5w, Feld6w, Feld7w, guinea pig (Cavp1, Cavp2); Mouse Urinary Protein (MUP, Musm1) allergen, Mus m 1, Rat Urinary Protein (RUP, Ratn1) allergen, Rat n 1., Equus caballus (Equc2.0101, Equc2.0102)) Insects Mosquito (Aeda1, Aeda2); honey bee (Apim1, Apim2, Apim4, Apim6, Apim7); bumble bee (Bomp1, Bomp4); German cockroach (Blag1, Blag2, Blag4, Blag5, Blag6, Blag7, Blag8); American cockroach (Pera1, Pera3, Pera6, Pera7); midge (Chit1-9, Chit1.01, Chit1.02, Chit2.0101, Chit2.0102, Chit3, Chit4, Chit5, Chit6.01, Chit6.02, Chit7, Chit8, Chit9); cat flea (Ctef1, Ctef2, Ctef3); pine processionary moth (Thap1); silverfish (Leps1); white face hornet (Dolm1, Dolm2, Dolm5); yellow hornet (Dola5); wasp (Pola1, Pola2, Pola5, Pole1, Pole5, Polf5, Polg5, Polm5, Vesvi5); Mediterranean paper wasp (Pold1, Pold4, Pold5); European hornet (Vespc1, Vespc5); giant asian hornet (Vespm1, Vespm5); yellowjacket (Vesf5, Vesg5, Vesm1, Vesm2, Vesm5, Vesp5, Vess5, Vesv1, Vesv2, Vesv5); Australian jumper ant (Myrp1, Myrp2); tropical fire ant (Solg2, Solg4); fire ant (Soli2, Soli3, Soli4); Brazilian fire ant (Sols2); California kissing bug (Triap1); Blattella germanica (Blag1.0101, Blag1.0102, Blag1.0103, Blag1.02, Blag6.0101, Blag6.0201, Blag6.0301); Periplaneta Americana (Pera1.0101, Pera1.0102, Pera1.0103, Pera1.0104, Pera1.02, Pera3.01, Pera3.0201, Pera3.0202, Pera3.0203, Pera7.0101, Pera7.0102); Vespa crabo (Vespc5.0101, Vespc5.0101); and Vespa mandarina (Vesp m 1.01, Vesp m 1.02) Rubber rubber (latex)(Hevb1, Hevb2, Hevb3, Hevb4, Hevb5, Hevb6.01, Hevb6.02, Hevb6.03, Hevb7.01, Hevb7.02, Hevb8, Hevb9, Hevb10, Hevb11, Hevb12, Hevb13); Hevea brasiliensis (Hevb6.01, Hevb6.0201, Hevb6.0202, Hevb6.03, Hevb8.0101, Hevb8.0102, Hevb8.0201, Hevb8.0202, Hevb8.0203, Hevb8.0204, Hevb10.0101, Hevb10.0102, Hevb10.0103, Hevb11.0101, Hevb11.0102) Others Nematode (Anis1, Anis2, Anis3, Anis4); pigeon tick (Argr1); worm (Ascs1); papaya (Carp1); soft coral (Denn1); human autoallergens (Homs1, Homs2, Homs3, Homs4, Homs5); obeche (Trips1)

TABLE B6 Infectious Agent-derived Epitopes Infectious Agent Epitope Mycobacterium tuberculosis isocitrate dehydrogenase (ICDs) Influenza virus Hemagglutinin (H1), neuraminidase (N1) Dengue virus envelope (E) Toxoplasma gondii microneme proteins, SAG1, SAG2, GRA1, GRA2, GRA4, GRA6, GRA7, GRA3, ROP1, ROP2, p30, MIC3, MIC2, M2AP, p29, p35, p66 Entamoeba histolytica M17, neutral thiol proteinase Streptococcus pneumonia Pneumolysin, pneumococcal histidine triad D (PhtD), pneumococcal choline-binding protein A (PcpA), pneumococcal histidine triad E (PhtE), LytB Mycoplasma pneumonia exotoxin Epstein-Barr virus VCA Helicobacter pylori CagA, Vacuolating protein, ureB, hsp60, ureH, urea, ferritin like protein Campylobacter jejuni PEB1, PEB3 Bacillus anthracis SAP SARS virus RNA-dependent replicases Ia and Ib, spike (S) protein, small envelope (E) protein, membrane (M) protein, and nucleocapsid (N) protein Ebola virus Nucleoprotein N Schmallenberg virus N nucleoprotein enterovirus 71 VPI protein Japanese Encephalitis virus soluble E protein, envelope E protein Ross River virus soluble E2 protein Mayaro virus soluble E2 protein Equine Encephalitis viruses soluble E2 protein Akabane virus N nucleoprotein human betacoronavirus Nucleoprotein N, protein S Hepatitis C virus protein C, core antigen Hepatitis E virus protein C Plasmodium falciparum MSP-1 + AMA-1 protein Leptospira interrogans HbpA, LruA, LruB, or LipL32

In some instances, the biomarker to be detected using the present method is a micro RNA (miRNA) biomarker that is associated with a disease or a health condition. The following Table B7 provides a list of miRNA biomarker that can be detected using the present invention, and their associated diseases/health conditions.

TABLE B7 Diagnostic miRNA Markers Disease/Condition Marker* Breast cancer miR-10b, miR-21, miR-125b, miR-145, miR-155, miR-191, miR-382, MiR-1, miR-133a, miR-133b, miR-202, miR-1255a, miR-671-3p, miR- 1827, miR-222, miR-744, miR-4306, miR-151-3p, miR-130, miR-149, miR-652, miR-320d, miR-18a, miR-181a, miR-3136, miR-629, miR-195, miR-122, miR-375, miR-184, miR-1299, miR381, miR-1246, miR-410, miR-196a, miR-429, miR-141, miR-376a, miR-370, miR-200b, miR- 125a-5p, miR-205, miR-200a, miR-224, miR-494, miR-216a, miR-654- 5p, miR-217, miR-99b, miR-885-3p, miR-1228, miR-483-5p, miR-200c, miR-3065-5p, miR-203, miR-1308, let-7a, miR-17-92, miR-34a, miR- 223, miR-150, miR-15b, miR-199a-5p, miR-33a, miR-423-5p, miR-424, let-7d, miR-103, miR-23b, miR-30d, miR-425, miR-23a, miR-26a, miR- 339-3p, miR-127-3p, miR-148b, miR-376a, miR-376c, miR-409-3p, miR-652, miR-801 (miR-92a, miR-548d-5p, miR-760, miR-1234, miR-18b, miR-605, miR- 193b, miR-29) Leukemia miR-98, miR-155, miR-21, let-7, miR-126, miR-196b, miR-128, miR- 195, miR-29a, miR-222, miR-20a, miR-150, miR-451, miR-135a, miR- 486-5p, miR-92, miR-148a, miR-181a, miR-20a, miR-221, miR-625, miR-99b (miR-92a, miR-15, miR-16, miR-15a, miR-16-1, miR-29) Multiple myeloma miR-15a, miR-16, miR-193b-365, miR-720, miR-1308, miR-1246, miR- 1, miR-133a, miR-221, miR-99b, Let-7e, miR-125a-5p, miR-21, miR- 181a/b, miR-106b-25, miR-32, miR-19a/b, miR-17-92, miR-17, miR-20, miR-92, miR-20a, miR-148a, miR-153, miR-490, miR-455, miR-642, miR-500, miR-296, miR-548d, miR-373, miR-554, miR-888, miR-203, miR-342, miR-631, miR-200a, miR-34c, miR-361, miR-9*, miR-200b, miR-9, miR-151, miR-218, miR-28-3p, miR-200c, miR-378, miR-548d- 5p, miR-621, miR-140-5p, miR-634, miR-616, miR-130a, miR-593, miR- 708, miR-200a*, miR-340, miR-760, miR-188-5p, miR-760, miR-885-3p, miR-590-3p, miR-885-5p, miR-7, miR-338, miR-222, miR-99a, miR- 891a, miR-452, miR-98, miR-629, miR-515-3p, miR-192, miR-454, miR- 151-3p, miR-141, miR-128b, miR-1227, miR-128a, miR-205, miR-27b, miR-608, miR-432, miR-220, miR-135a, miR-34a, miR-28, miR-412, miR-877, miR-628-5p, miR-532-3p, miR-625, miR-34b, miR-31, miR- 106b, miR-146a, miR-210, miR-499-5p, miR-140, miR-188, miR-610, miR-27a, miR-142-5p, miR-603, miR-660, miR-649, miR-140-3p, miR- 300, miR-335, miR-206, miR-20b, miR-130b, miR-183, miR-652, miR- 133b, miR-191, miR-212, miR-194, miR-100m miR-1234m miR-182m miR-888, miR-30e-5p, miR-574, miR-135b, miR-125b, miR-502m miR- 320, miR548-421, miR-129-3p, miR-190b, miR-18a, miR-549, 338-5p, miR-756-3p, miR-133a, miR-521, miR-486-3p, miR-553, miR-452*, miR-628-3p, miR-620, miR-566, miR-892a, miR-miR-339-5p, miR-628, miR-520d-5p, miR-297, miR-213, miR-519e*, miR-422a, miR-198, miR- 122a, miR-1236, miR-548c-5p, miR-191*, miR-583, miR-376c, miR-34c- 3p, miR-453, miR-509, miR-124a, miR-505, miR-208, miR-659, miR- 146b, miR-518c, miR-665, miR-324-5p, miR-152, miR-548d, miR-455- 3p (miR-15a, miR-373*, miR-378*, miR-143, miR-337, miR-223, miR-369- 3p, miR-520g, miR-485-5p, miR-524, miR-520h, miR-516-3p, miR- 519d, miR-371-3p, miR-455, miR-520b, miR-518d, miR-624, miR-296, miR-16) monoclonal miR-21, miR-210, miR-9*, miR-200b, miR-222, miR-376 gammopathy of (miR-339, miR-328) undetermined significance Myelodisplastic (Let-7a, miR-16) syndrome Lymphoma miR-155, miR-210, miR-21, miR-17-92, miR-18a, miR-181a, miR-222, miR-20a/b, miR-194, miR-29, miR-150, miR-155, miR-223, miR-221, let-7f, miR-146a, miR-15, miR-16-1, miR-34b/c, miR-17-5p (miR-20b, miR-184, miR-200a/b/c, miR-205, miR-34a, miR-29a, miR- 29b-1, miR-139, miR-345, miR-125a, miR-126, miR-26a/b, miR-92a, miR-20a, miR-16, miR-101, miR-29c miR-138, miR-181b) Lung cancer let-7c, miR-100, miR-10a, miR-10b, miR-122a, miR-125b, miR-129, miR-148a, miR-150, miR-17-5p, miR-183, miR-18a*, miR-18b, miR-190, miR-192, miR-193a, miR-196b, miR-197, miR-19a, miR-19b, miR-200c, miR-203, miR-206, miR-20b, miR-210, miR-214, miR-218, miR-296, miR-30a-3p, miR-31, miR-346, miR-34c, miR-375, miR-383, miR-422a, miR-429, miR-448, miR-449, miR-452, miR-483, miR-486, miR-489, miR-497, miR-500, miR-501, miR-507, miR-511, miR-514, miR-516-3p, miR-520d, miR-527, miR-7, miR-92, miR-93, miR-99a, miR-25, miR- 223, miR-21, miR-155, miR-556, miR-550, miR-939, miR-616*, miR- 146b-3p and miR-30c-1*, miR-142-5p, miR-328, miR-127, miR-151, miR-451, miR-126, miR-425-5p, miR-222, miR-769-5p, miR-642, miR- 202, miR-34a (let-7a, let-7d, let-7e, let-7g, let-7i, miR-1, miR-103, miR-106a, miR- 125a, miR-130a, miR-130b, miR-133a, miR-145, miR-148b, miR-15a, miR-15b, miR-17-3p, miR-181d, miR-18a, miR-196a, miR-198, miR- 199a, miR-199a*, miR-212, miR-22, miR-221, miR-23a, miR-23b, miR- 26a, miR-27a, miR-27b, miR-29b, miR-30b, miR-30d, miR-30e-3p, miR- 320, miR-323, miR-326, miR-331, miR-335, miR-339, miR-374, miR- 377, miR-379, miR-410, miR-423, miR-433, miR-485-3p, miR-485-5p, miR-487b, miR-490, miR-491, miR-493, miR-493-3p, miR-494, miR- 496, miR-502, miR-505, miR-519d, miR-539, miR-542-3p, miR-98) Colorectal cancer miR-29a, miR-17-3p, miR-92, miR-21, miR-31, miR-155, miR-92a, miR- 141, mir-202, mir-497, mir-3065, mir-450a-2, mir-3154, mir-585, mir- 3175, mir-1224, mir-3117, mir-1286 (miR-34) Prostate cancer miR-141, miR-375, miR-16, miR-92a, miR-103, miR-107, miR-197, miR- 485-3p, miR-486-5p, miR-26a, miR-92b, miR-574-3p, miR-636, miR- 640, miR-766, miR-885-5p, miR-141, miR-195, miR-375, miR-298, miR- 346, miR-1-1, miR-1181, miR-1291, miR-133a-1, miR-133b, miR-1469, miR-148*, miR-153, miR-182, miR-182*, miR-183, miR-183*, miR-185, miR-191, miR-192, miR-1973, miR-200b, miR-205, miR-210, miR-33b*, miR-3607-5p, miR-3621, miR-378a, miR-429, miR-494, miR-582, miR- 602, miR-665, miR-96, miR-99b*, miR-100, miR-125b, miR-143, miR- 200a, miR-200c, miR-222, miR-296, and miR-425-5p Ovarian cancer miR-21, miR-92, miR-93, miR-126, miR-29a, miR-141, miR-200a/b/c, miR-203, miR-205, miR-214, miR-221, miR-222, miR-146a, miR-150, miR-193a-5p, miR-31, miR-370, let-7d, miR-508-5p, miR-152, miR- 509-3-5p, miR-508-3p, miR-708, miR-431, miR-185, miR-124, miR-886- 3p, hsa-miR-449, hsa-miR-135a, hsa-miR-429, miR-205, miR-20b, hsa- miR-142-5p, miR-29c, miR-182 (miR-155, miR-127, miR-99b) Cervical cancer miR-21, miR-9, miR-200a, miR-497 (miR-143, miR-203, miR-218) Esophageal miR-21, hsa-miR-200a, hsa-miR-345, hsa-miR-373*, hsa-miR-630, hsa- carcinoma miR-663, hsa-miR-765, hsa-miR-625, hsa-miR-93, hsa-miR-106b, hsa- miR-155, hsa-miR-130b, hsa-miR-30a, hsa-miR-301a, hsa-miR-15b (miR-375) Gastric cancer miR-17-5p, miR-21, miR-106a, miR-106b, miR-187, miR-371-5p, miR- 378 (let-7a, miR-31, miR-192, miR-215, miR-200/141) Pancreatic cancer, miR-210, miR-21, miR-155, miR-196a, miR-1290, miR-20a, miR-24, ductal miR-25, miR-99a, miR-185, miR-191, miR-18a, miR-642b-3p, miR-885- adenocarcinoma 5p, miR-22-3p, miR-675, miR-212, miR-148a*, miR-148, miR-187, let- 7g*, miR-205, miR-944, miR-431, miR-194*, miR-769-5p, miR-450b-5p, miR-222, miR-222*, miR-146, miR-23a*, miR-143*, miR-216a, miR- 891a, miR-409-5p, miR-449b, miR-330-5p, miR-29a*, miR-625 Hepatocellular miR-500, miR-15b, miR-21, miR-130b, miR-183, miR-122, miR-34a, carcinoma miR-16, miR-221, miR-222 Melanoma miR-150, miR-15b, miR-199a-5p, miR-33a, miR-423-5p, miR-424, miR- let-7d, miR-103, miR-23b, miR-30d, miR-425, miR-222, miR-23a, miR- 26a, miR-339-3p Squamous cell miR-184a carcinoma Bladder cancer miR-126, miR-182 (urine), miR-16, miR-320 (miR-143, miR-145, miR-200/141) Renal cancer miR-1233, miR-199b-5p, miR-130b (miR-10b, miR-139-5p) Oral cancer miR-31, miR-24, miR-184; miR-34c; miR-137; miR-372; miR-124a; miR- 21; miR-124b; miR-31; miR-128a; miR-34b; miR-154; miR-197; miR- 132; miR-147; miR-325; miR-181c; miR-198; miR-155; miR-30a-3p; miR-338; miR-17-5p; miR-104; miR-134; miR-213 (miR-200a, miR-125a, miR-133a; miR-99a; miR-194; miR-133; miR- 219; miR-100; miR-125; miR-26b; miR-138; miR-149; miR-195; miR- 107; and miR-139 (saliva)) Head and neck miR-455-3p, miR-455-5p, miR-130b, miR-130b*, miR-801, miR-196a, cancer miR-21, miR-31 Endometrial cancer miR-503, miR-424, miR-29b, miR-146a, miR-31 Testicular cancer miR-372, miR-373 Glioblastoma miR-21, miR-221, miR-222 Thyroid cancer miR-187, miR-221, miR-222, miR-146b, miR-155, miR-224, miR-197, miR-192, miR-328, miR-346, miR-512-3D, miR-886-5p, miR-450a, miR- 301 b, miR-429, miR-542-3p, miR-130a, miR-146b-5p, miR-199a-5p, miR-193a-3p, miR-152, miR-199a-3p/miR-199b-3p, miR-424, miR-22, miR-146a, miR-339-3p, miR-365, let-7i*, miR-363*, miR-148a, miR-299- 3p, let-7a*, miR-200b, miR-200c, miR-375, miR-451, miR-144, let-7i, miR-1826, miR-1201, miR-140-5p, miR-126, miR-126*, let-7f-2*, miR- 148b, miR-21*, miR-342-3p, miR-27a, miR-145*, miR-513b, miR-101, miR-26a, miR-24, miR-30a*, miR-377, miR-518e7, miR-519a7, miR- 519b-5p, miR-519c-5p, miR-5227, miR-523*, miR-222*, miR-452, miR- 665, miR-584, miR-492, miR-744, miR-662, miR-219-2-3p, miR-631 and miR-637, miRPlus-E1078, miR-19a, miR-501-3p, miR-17, miR-335, miR-106b, miR-15a, miR-16, miR-374a, miR-542-5p, miR-503, miR- 320a, miR-326, miR-330-3p, miR-1, miR-7b, miR-26b, miR-106a, miR-139, miR-141, miR-143, miR- 149, miR-182, miR-190b, miR-193a, miR-193b, miR-211, miR-214, miR-218, miR-302c*, miR-320, miR-324, miR-338, miR-342, miR-367, miR-378, miR-409, miR-432, miR-483, miR-486, miR-497, miR-518f, miR-574, miR-616, miR-628, miR-663b, miR-888, miR-1247, miR-1248, miR-1262, and miR-1305 miR-21, miR-25, miR-32, miR-99b*, miR-125a, miR-125b, miR-138, miR-140, miR-181a, miR-213, miR-221, miR-222, and miR-345 Ischemic heart miR-1, miR-30c, miR-133, miR-145, miR-208a/b, miR-499, miR-663b, disease/Myocardial miR-1291 infarction (miR-126, miR-197, miR-223) Heart failure miR-29b, miR-122, miR-142-3p, miR-423-5p, miR-152, miR-155, miR- 497 (miR-107, miR-125b, miR-126, miR-139, miR-142-5p, miR-497) Stroke miR-124, miR-145 (miR-210) Coronary artery miR-21, miR-27b, miR-130a, miR-134, miR-135a, miR-198, miR-210, disease miR-370 (miR-17, miR-92a, miR-126, miR-145m miR-155m miR-181a, miR-221, miR-222) Diabetes miR-9, miR-28-3p, miR-29a, miR-30d, miR-34a, miR-124a, miR-146a, miR-375, miR-503, 144 (miR-15a, miR-20b, miR-21, miR-24, miR-126, miR-191, miR-197, 223, miR-320, miR-486) Hypertension Hcmv-miR-UL112, Let-7e (miR-296-5p) Chronic HCV miR-155, miR-122, miR-125b, miR-146a, miR-21 infection Liver injury miR-122, miR-192 Sepsis miR-146a, miR223 Arthritis miR-125a-5p, miR-24, miR-26a, miR-9, miR-25, miR-98, miR-146a, miR-124a, miR-346, miR-223, miR-155 (miR-132, miR-146) Systemic lupus (miR-200a/b/c, miR-205, miR-429, miR-192, miR-141, miR-429, miR- erythematosus 192 (urine or serum)) Chron disease miR-199a-5p, miR-362-3p, miR-532-3p, miR-plus-E1271, miR-340* (miR-149*, miR-plus-F1065) Ulcerative colitis miR-28-5p, miR-151-5p, miR-199-5p, miR-340*, miR-plus-E1271, miR- 103-2*, miR-362-3p, miR-532-3p (miR-505) Asthma miR-705, miR-575, let-7d, miR-173p, miR-423-5p, miR-611, miR-674, let-7f-1, miR-23b, miR-223, miR-142-3p, let-7c, miR-25, miR-15b, let- 7g, and miR-542-5p, miR-370 (miR-325, miR-134, miR-198, miR-721, miR-515-3p, miR-680, miR-601, miR-206, miR-202, miR-671, miR-381, miR-630, miR-759, miR-564, miR-709, miR-513, miR-298) Chronic pulmonary miR-148a, miR-148b, miR-152 disease Idiopathic miR-199a-5p pulmonary fibrosis Alzheimer's disease (miR-137, miR-181c, miR-9, miR-29a/b) Duchenne muscular miR-1, miR-133a, miR-206 dystrophy Multiple sclerosis miR-633, miR-181c-5p (CSF), miR-17-5p, miR-193a, miR-326, miR- 650, miR-155, miR-142-3p, miR-146a, miR-146b, miR-34a, miR-21, miR-23a, miR-199a, miR-27a, miR-142-5p, miR-193a, miR-15a, miR- 200c, miR-130a, miR-223, miR-22, miR-320, miR-214, miR-629, miR- 148a, miR-28, miR-195, miR-135a, miR-204, miR-660, miR-152, miR- 30a-5p, miR-30a-3p, miR-365, miR-532, let-7c, miR-20b, miR-30d, miR- 9, hsa-mir-18b, hsa-mir-493, hsa-mir-599, hsa-mir-96, hsa-mir-193, hsa-mir-328, hsa-mir-409-5p, hsa-mir-449b, hsa-mir-485-3p, hsa-mir- 554 (miR-922 (CSF), miR-497, miR-1 and miR-126, miR-656, miR-184, miR-139, miR-23b, miR-487b, miR-181c, miR-340, miR-219, miR-338, miR-642, miR-181b, miR-18a, miR-190, miR-213, miR-330, miR-181d, miR-151, miR-140) Preeclampsia miR-210 (miR-152) Gestational diabetes (miR-29a, miR-132) Platelet activity miR-126, miR-197, miR-223, miR-24, miR-21 Pregnancy/placenta- miR-526a, miR-527, miR-520d-5p, miR-141, miR-149, miR-299-5p, derived miR-517a Drug treatment for miR-130a, miR-146b, miR-143, miR-145, miR-99b, miR-125a, miR-204, immunomodulation miR-424, miR-503 Aging (miR-151a-3p, miR-181a-5p, miR-1248) *miRNA markers in parentheses are downregulated Environmental Testing.

As summarized above, the devices, systems and methods in the present invention can find use in analyzing an environmental sample, e.g., a sample from water, soil, industrial waste, etc., for the presence of environmental markers. An environmental marker can be any suitable marker, that can be captured by a capturing agent that specifically binds the environmental marker in a CROF device configured with the capturing agent. The environmental sample can be obtained from any suitable source, such as a river, ocean, lake, rain, snow, sewage, sewage processing runoff, agricultural runoff, industrial runoff, tap water or drinking water, etc. In some embodiments, the devices and systems in the present invention detect the concentration of lead or toxins in water. In some embodiments, the presence or absence, or the quantitative level of the environmental marker in the sample can be indicative of the state of the environment from which the sample was obtained. In some cases, the environmental marker can be a substance that is toxic or harmful to an organism, e.g., human, companion animal, plant, etc., that is exposed to the environment. In some cases, the environmental marker can be an allergen that can cause allergic reactions in some individuals who are exposed to the environment. In some instances, the presence or absence, or the quantitative level of the environmental marker in the sample can be correlated with a general health of the environment. In such cases, the general health of the environment can be measured over a period of time, such as week, months, years, or decades.

In some embodiments, the devices, systems and methods in the present invention further includes receiving or providing a report that indicates the safety or harmfulness for a subject to be exposed to the environment from which the sample was obtained based on information including the measured amount of the environmental marker. The information used to assess the safety risk or health of the environment can include data other than the type and measured amount of the environmental marker. These other data can include the location, altitude, temperature, time of day/month/year, pressure, humidity, wind direction and speed, weather, etc. The data can represent an average value or trend over a certain period (minutes, hours, days, weeks, months, years, etc.), or an instantaneous value over a shorter period (milliseconds, seconds, minutes, etc.).

The report can be generated by the device configured to read the CROF device, or can be generated at a remote location upon sending the data including the measured amount of the environmental marker. In some cases, an expert can be at the remote location or have access to the data sent to the remote location, and can analyze or review the data to generate the report. The expert can be a scientist or administrator at a governmental agency, such as the US Centers for Disease Control (CDC) or the US Environmental Protection Agency (EPA), a research institution, such as a university, or a private company. In certain embodiments, the expert can send to the user instructions or recommendations based on the data transmitted by the device and/or analyzed at the remote location.

A list of exemplary environmental markers is set forth in Table 8 of U.S. provisional application Ser. No. 62/234,538, filed on Sep. 29, 2015, which application is incorporated by reference herein.

TABLE B8 Environmental Markers Class/Source Marker Synthetic 17beta-estradiol (E2), estrone (EI), estrogen (ES: EI + E2 + estriol (E3)), 1 hormone 7alfa-ethynylestradiol (EE2), 4-nonylphenpol, testosterone analogues Halogenated p,p′-DDE, p,p′-DDD, p,p′-DDT, o,p′-DDE, o,p′-DDE, o,p′-DDT, o,p′-DDD, hydrocarbons chlordane, nonachlor, oxychlordane, heptachlor, heptachlor epoxide, pentachloroanisole, hexachlorobenzene, heptachlorbenzene, o,p′- methoxychlor, p,p′-methoxychlor, Hexachlorocyclopentadiene Pesticides manganese ethylene-bis-dithiocarbamate, diazinon, chlorphyrifos, carbofuran, carbaryl, malathion, dieldrin, fipronil, desulfinylfipronil, fipronil sulfide, fipronil sulfone, aldicarb, aldicarb sulfone, aldicarb sulfoxide, carbaryl, 3- hydroxycarbofuran, methiocarb, methomyl, , oxamyl, propoxur, alpha-HCH, gamma-HCH, beta-HCH, delta-HCH, azinphos-methyl, chlorpyrifos, disulfoton, parathion, fonofos, ethoprop, parathion-methyl, phorate, terbufos, cis- permethrin, trans-permethrin, propargite, aldrin, chloroneb, endosulfan I, endrin, isodrin, mirex, toxaphene, lindane, O-ethyl O-4-nitrophenyl phenylphosphono-thioate (EPN), fenitrothion, pirimiphos-methyl, deltamethrin Herbicide acetochlor, alachlor, metolachlor, atrazine, deethylatrazine, cyanazine, terbuthylazine, terbutryn, metribuzin, bentazon, EPTC, triflualin, molinate norflurazon, simazine, prometon, promteryn, tebuthiuron, 2,4-D, diuron, dacthal, bromacil, deisopropyl atrazine, hydroxyatrazine, deethylhydroxyatrazine, deisopropylhydroxyatrazine, acetochlor ESA, acetochlor OA, alachlor ESA, alachlor OA, metolachlor ESA, metolachlor OA, 2,6-diethylaniline, napropamide, pronamide, propachlor, propanilm butylate, pebulate, propham, thiobencarb, triallate, dacthal, dacthal monoacid, 2,4-DB, dischlorprop, MCPA, MCPB, 2,4,5-T, 2,4,5-TP, benfluralin, ethalfluralin, oryzalin, pendimethalin, trifluralin, bentazon, norflurazon, acifluorfen, chloramben methyl ester, clopyralid, dicamba, picloram, dinoseb, DNOC, chlorothalonil, dichlobenil, 2,6-dichlorobenzamide (BAM), triclopyr, bromoxynil, bromacil, terbacil, fenuron, fluometuron, linuron, neburon, dalapon, diquat, endothall, Glyphosate, N-dealkylated triazines, mecoprop Industrial chromated copper arsenate, Carbon tetrachloride, Chlorobenzene, p- material/waste Dichlorobenzene, 1,2-Dichloroethanem, 1,1-Dichloroethylene, cis-1,2- Dichloroethylene, trans-1,2-Dichloroethylene, Dichloromethane, Di(2- ethylhexyl) adipate, Di(2-ethylhexyl) phthalate, Dibutyl phthalate (DBP), diethyl phthalate (DEP), dicyclohexyl phthalate (DCHP), Dioxin (2,3,7,8-TCDD), Epichlorohydrin, Ethylene dibromide, Polychlorinated biphenyls, Pentachlorophenol, styrene, Tetrachloroethylene, Toluene diisocyanate (TDI), 1,2,4-Trichlorobenzene, 1,1,1-Trichloroethane, 1,1,2-Trichloroethane, Trichloroethylene, perchloroethylene, Vinyl chloride, Xylenes, alkylphenol (AP), AP + APE, bisphenol A (BPA), benzene, Xylene, Toluene, Styrene, Toluidine, 2-(p-Tolyl)ethylamine, Ethylbenzene, 2-Methyl-naphthalene, and Propyl-benzene, PAH (polynuclear aromatic hydrocarbons) Drinking water Bromate, Chlorite, Haloacetic acids, Total Trihalomethanes, Chloramines, Chlorine, Chlorine dioxide, Benzo(a)pyrene, 4-tert-octylphenol Household Acrylamide, linear alkylbenzene sulfonates (LAS), alkyl ethoxylates (AE), waste/Sewage alkylphenol ethoxylates (APE), triclosan runoff Poison/toxins N-methylamino-L-alanine (BMAA), Clostridium botulinum neurotoxins, BoNT A, B, D, E, Ricin A, B, tetanus toxin, diphtheria toxin, pertussis toxin Heavy metal mercury/methylmercury, lead/tetraethyl lead, zinc, copper, nickel, cadmium, chromium(VI)/chromate, aluminum, iron, arsenic, cobalt, selenium, silver, antimony, thallium, polonium, radium, tin, metallothionein (in carp liver tissue) Other Lithium, beryllium, manganese, barium, cyanide, fluoride metals/inorganic chemicals Pathogens/microbes Anthrax (LF), Giardia lamblia, Legionella, Total Coliforms (including fecal (antigen in coliform and E. Coli), Viruses (enteric) stapylococci (e.g., Staphylococcus pretheses) epidermidis and Staphylococcus aureus (enterotoxin A, B, C, G, I, cells, TSST-1), Enterrococcus faecalis, Pseudomonas aeruginosa, Escherichia coli (Shiga-like toxin, F4, F5, H, K, O, bacteriophage K1, K5, K13), other gram- positive bacteria, and gram-negative bacilli. Clostridium difficile (Toxin A, B) Bacteroidetes, Cryptosporidium parvum (GP900, p68 or cryptopain, oocyst), Candida albicans Bacillus anthracis, Bacillus stearothermophilus Norovirus, Listeria monocytogenes (internalin), Leptospira interrogans, Leptospira biflexa, Clostridium perfringens (Epsilon toxin), Salmonella typhimurium, Yersinia pestis (F1, V antigens), Aspergillus flavus (aflatoxin), Aspergillus parasiticus (aflatoxin), avian influenza virus, Ebola virus (GP), Histoplasma capsulatum, Blastomyces dermatitidis (A antigen) Gram-positive bacteria (teichoic acid), Gram-ngative bacteria (such as Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella enteriditis, Enterobacter aerogenes, Enterobacter hermanii, Yersinia enterocolitica and Shigella sonnei)(LPS), Polio virus, Influenza type A virus Disease specific prion (PrP-d) Allergens mite (Acas13, Blot1, Blot3, Blot4, Blot5, Blot6, Blot10, Blot11, Blot12, Blot13, Blot19); American house dust mite (Derf1, Derf2, Derf3, Derf7, Derf10, Derf11, Derf14, Derf15, Derf16, Derf17, Derf18w); house dust mite (Derm1); European house dust mite (Derp1, Derp2, Derp3, Derp4, Derp5, Derp6, Derp7, Derp8, Derp9, Derp10, Derp11, Derp14, Derp20, Derp21); mite (Eurm2; Eurm14); storage mite (Glyd2, Lepd2, Lepd5, Lepd7, Lepd10, Lepd13, Tyrp2, Tyrp13); Dermatophagoides farinae (Derf1.0101, Derf1.0102, Derf1.0103, Derf1.0104, Derf1.0105, Derf2.0101, Derf2.0102, Derf2.0103, Derf2.0104, Derf2.0105, Derf2.0106, Derf2.0107, Derf2.0108, Derf2.0109, Derf2.0110, Derf2.0111, Derf2.0112, Derf2.0113, Derf2.0114, Derf2.0115, Derf2.0116, Derf2.0117); Dermatophagoides pteronyssinus (Derp1.0101, Derp1.0102, Derp1.0103, Derp1.0104, Derp1.0105, Derp1.0106, Derp1.0107, Derp1.0108, Derp1.0109, Derp1.0110, Derp1.0111, Derp1.0112, Derp1.0113, Derp1.0114, Derp1.0115, Derp1.0116, Derp1.0117, Derp1.0118, Derp1.0119, Derp1.0120, Derp1.0121, Derp1.0122, Derp1.0123, Derp2.0101, Derp2.0102, Derp2.0103, Derp2.0104, Derp2.0105, Derp2.0106, Derp2.0107, Derp2.0108, Derp2.0109, Derp2.0110, Derp2.0111, Derp2.0112, Derp2.0113); Euroglyphus maynei (Eurm2.0101, Eurm2.0102); Glycyphagus domesticus (Glyd2.0101, Glyd2.0201); and Lepidoglyphus destructor (Lepd2.0101, Lepd2.0101, Lepd2.0101, Lepd2.0102, Lepd2.0201, Lepd2.0202) Pollen (Short Ragweed (Ambrosia artemisiifolia) allergen, Amb a 1, Amba2, Amba3, Amba5, Amba6, Amba7, Amba8, Amba9, Arnba10; Betula verrucosa allergen, Bet v 1, Phleum pratense allergen, Phl p 5), giant ragweed (Ambt5); mugwort (Artv1, Artv2, Artv3, Artv4, Artv5, Artv6); sunflower (Hela1, Hela2, Hela3); Mercurialis annua (Mera1); lamb's-quarters, pigweed (Chea1); white goosefoot (Chea2, Chea3); Russian-thistle (Salk1); Rosy periwinkle (Catr1); English plantain (Plal1); Japanese hop (Humj1); Parietaria judaica (Parj1, Parj2, Parj3); Parietaria officinalis (Paro1); Ambrosia artemisiifolia (Amba8.0101, Amba8.0102, Amba9.0101, Amba9.0102); Plantago lanceolata (Plal1.0101, Plal1.0102, Plal1.0103); and Parietaria judaica (Parj1.0101, Parj1.0102, Parj1.0201, Par2.0101, Parj2.0102, Parj3.0101, Parj3.0102), Bermuda grass (Cynd1, Cynd7, Cynd12, Cynd15, Cynd22w, Cynd23, Cynd24); orchard grass (Dacg1, Dacg2, Dacg3, Dacg5); meadow fescue (Fesp4w); velvet grass (HolH); rye grass (Lolp1, Lolp2, Lolp3, Lolp5, Lolp11); canary grass (Phaa1); Timothy (Phlp1, Phlp2, Phlp4, Phlp5, Phlp6, Phlp11, Phlp12, Phlp13); Kentucky blue grass (Poap1, Poap5); Johnson grass (Sorh1); Cynodon dactylon (Cynd1.0101, Cynd1.0102, Cynd1.0103, Cynd1.0104, Cynd1.0105, Cynd1.0106, Cynd1.0107, Cynd1.0201, Cynd1.0202, Cynd1.0203, Cynd1.0204); Holcus lanatus (Holl1.0101, Holl1.0102); Lolium perenne (Lolp1.0101, Lolp1.0102, Lolp1.0103, Lolp5.0101, Lolp5.0102); Phleum pretense (Phlp1.0101, Phlp1.0102, Phlp4.0101, Phlp4.0201, Phlp5.0101, Phlp5.0102, Phlp5.0103, Phlp5.0104, Phlp5.0105, Phlp5.0106, Phlp5.0107, Phlp5.0108, Phlp5.0201, Phlp5.0202); and Secale cereale (Secc20.0101, Secc20.0201), Alder (Alng1); Birch (Betv1, Betv2, Betv3, Betv4, Betv6, Betv7); hornbeam (Carb1); chestnut (Cass1, Cass5, Cass8); hazel (Cora1, Cora2, Cora8, Cora9, Coral0, Cora11); White oak (Quea1); Ash (Frae1); privet (Ligv1); olive (Olee1, Olee2, Olee3, Olee4, Olee5, Olee6, Olee7, Olee8, Olee9, Olee10); Lilac (Syrv1); Sugi (Cryj1, Cryj2); cypress (Cupa1); common cypress (Cups1, Cups3w); mountain cedar (Juna1, Juna2, Juna3); prickly juniper (Juno4); mountain cedar (Juns1); eastern red cedar (Junv1); London plane tree (Plaa1, Plaa2, Plaa3); date palm (Phod2); Betula verrucosa (Betv1.0101, Betv1.0102, Betv1.0103, Betv1.0201, Betv1.0301, Betv1.0401, Betv1.0402, Betv1.0501, Betv1.0601, Betv1.0602, Betv1.0701, Betv1.0801, Betv1.0901, Betv1.1001, Betv1.1101, Betv1.1201, Betv1.1301, Betv1.1401, Betv1.1402, Betv1.1501, Betv1.1502, Betv1.1601, Betv1.1701, Betv1.1801, Betv1.1901, Betv1.2001, Betv1.2101, Betv1.2201, Betv1.2301, Betv1.2401, Betv1.2501, Betv1.2601, Betv1.2701, Betv1.2801, Betv1.2901, Betv1.3001, Betv1.3101, Betv6.0101, Betv6.0102); Carpinus betulus (Carb1.0101, Carb1.0102, Carb1.0103, Carb1.0104, Carb1.0105, Carb1.0106, Carb1.0106, Carb1.0106, Carb1.0106, Carb1.0107, Carb1.0107, Carb1.0108, Carb1.0201, Carb1.0301, Carb1.0302); Corylus avellana (Cora1.0101, Cora1.0102, Cora1.0103, Cora1.0104, Cora1.0201, Cora1.0301, Cora1.0401, Cora1.0402, Cora1.0403, Cora1.0404); Ligustrum vulgare (Ligv1.0101, Ligv1.01.02); Olea europea (Olee1.0101, Olee1.0102, Olee1.0103, Olee1.0104, Olee1.0105, Olee1.0106, Olee1.0107); Syringa vulgaris (Syrv1.0101, Syrv1.0102, Syrv1.0103); Cryptomeria japonica (Cryj2.0101, Cryj2.0102); and Cupressus sempervirens (Cups1.0101, Cups1.0102, Cups1.0103, Cups1.0104, Cups1.0105) mold (Alternaria alternata allergen, Alt a 1, Alta3, Alta4, Alta5, Alta6, Alta7, Alta8, Alta10, Alta12, Alta13, Aspergillus fumigatus allergen, Asp f 1, Aspf2, Aspf3, Aspf4, Aspf5, Aspf6, Aspf7, Aspf8, Aspf9, Aspf10, Aspf11, Aspf12, Aspf13, Aspf15, Aspf16, Aspf17, Aspf18, Aspf22w, Aspf23, Aspf27, Aspf28, Aspf29); Aspergillus niger (Aspn14, Aspn18, Aspn25); Aspergillus oryzae (Aspo13, Aspo21); Penicillium brevicompactum (Penb13, Penb26); Penicillium chrysogenum (Pench13, Pench18, Pench20); Penicillium citrinum (Penc3, Penc13, Penc19, Penc22w, Penc24); Penicillium oxalicum (Peno18); Fusarium culmorum (Fuse1, Fusc2); Trichophyton rubrum (Trir2, Trir4); Trichophyton tonsurans (Trit1, Trit4); Candida albicans (Canda1, Canda3); Candida boidinii (Candb2); Psilocybe cubensis (Psic1, Psic2); shaggy cap (Copd, Copc2, Copc3, Copc5, Copc7); Rhodotorula mucilaginosa (Rhom1, Rhom2); Malassezia furfur (Malaf2, Malaf3, Malaf4); Malassezia sympodialis (Malas1, Malas5, Malas6, Malas7, Malas8, Malas9, Malas10, Malas11, Malas12, Malas13); Epicoccum purpurascens (Epip1); and Alternaria alternate (Alta1.0101, Alta1.0102), Aspergillus versicolor antigen, S. chartarum antigen), Cladosporium herbarum (Clah2, Clah5, Clah6, Clah7, Clah8, Clah9, Clah10, Clah12); Aspergillus flavus (Aspf113); animals (Bos domesticus dander allergen, Bos d 2, Bosd3, Bosd4, Bosd5, Bosd6, Bosd7, Bosd8, Bosd2.0101, Bosd2.0102, Bosd2.0103, Canis familiaris allergen, Can f 1, Canf2, Canf3, Canf4, Equus caballus allergen, Equc1, Equc2, Equc3, Equc4, Equc5, Felis domesticus allergen, Fel d 1, Feld2, Feld3, Feld4, Feld5w, Feld6w, Feld7w, guinea pig (Cavp1, Cavp2); Mouse Urinary Protein (MUP, Musm1) allergen, Mus m 1, Rat Urinary Protein (RUP, Ratn1) allergen, Rat n 1., Equus caballus (Equc2.0101, Equc2.0102)) Mosquito (Aeda1, Aeda2); honey bee (Apim1, Apim2, Apim4, Apim6, Apim7); bumble bee (Bomp1, Bomp4); German cockroach (Blag1, Blag2, Blag4, Blag5, Blag6, Blag7, Blag8); American cockroach (Pera1, Pera3, Pera6, Pera7); midge (Chit1-9, Chit1.01, Chit1.02, Chit2.0101, Chit2.0102, Chit3, Chit4, Chit5, Chit6.01, Chit6.02, Chit7, Chit8, Chit9); cat flea (Ctef1, Ctef2, Ctef3); pine processionary moth (Thap1); silverfish (Leps1); white face hornet (Dolm1, Dolm2, Dolm5); yellow hornet (Dola5); wasp (Pola1, Pola2, Pola5, Pole1, Pole5, Polf5, Polg5, Polm5, Vesvi5); Mediterranean paper wasp (Pold1, Pold4, Pold5); European hornet (Vespc1, Vespc5); giant asian hornet (Vespm1, Vespm5); yellowjacket (Vesf5, Vesg5, Vesm1, Vesm2, Vesm5, Vesp5, Vess5, Vesv1, Vesv2, Vesv5); Australian jumper ant (Myrp1, Myrp2); tropical fire ant (Solg2, Solg4); fire ant (Soli2, Soli3, Soli4); Brazilian fire ant (Sols2); California kissing bug (Triap1); Blattella germanica (Blag1.0101, Blag1.0102, Blag1.0103, Blag1.02, Blag6.0101, Blag6.0201, Blag6.0301); Periplaneta Americana (Pera1.0101, Pera1.0102, Pera1.0103, Pera1.0104, Pera1.02, Pera3.01, Pera3.0201, Pera3.0202, Pera3.0203, Pera7.0101, Pera7.0102); Vespa crabo (Vespc5.0101, Vespc5.0101); and Vespa mandarina (Vesp m 1.01, Vesp m 1.02) Nematode (Anis1, Anis2, Anis3, Anis4); pigeon tick (Argr1); worm (Ascs1); papaya (Carp1); soft coral (Denn1); rubber (latex)(Hevb1, Hevb2, Hevb3, Hevb4, Hevb5, Hevb6.01, Hevb6.02, Hevb6.03, Hevb7.01, Hevb7.02, Hevb8, Hevb9, Hevb10, Hevb11, Hevb12, Hevb13); human autoallergens (Homs1, Homs2, Homs3, Homs4, Homs5); obeche (Trips1); and Hevea brasiliensis (Hevb6.01, Hevb6.0201, Hevb6.0202, Hevb6.03, Hevb8.0101, Hevb8.0102, Hevb8.0201, Hevb8.0202, Hevb8.0203, Hevb8.0204, Hevb10.0101, Hevb10.0102, Hevb10.0103, Hevb11.0101, Hevb11.0102) Foodstuff Testing.

As summarized above, the devices, systems and methods in the present invention can find use in analyzing a foodstuff sample, e.g., a sample from raw food, processed food, cooked food, drinking water, etc., for the presence of foodstuff markers. A foodstuff marker can be any suitable marker, such as those shown in Table B9, below, that can be captured by a capturing agent that specifically binds the foodstuff marker in a CROF device configured with the capturing agent. The environmental sample can be obtained from any suitable source, such as tap water, drinking water, prepared food, processed food or raw food, etc. In some embodiments, the presence or absence, or the quantitative level of the foodstuff marker in the sample can be indicative of the safety or harmfulness to a subject if the food stuff is consumed. In some embodiments, the foodstuff marker is a substance derived from a pathogenic or microbial organism that is indicative of the presence of the organism in the foodstuff from which the sample was obtained. In some embodiments, the foodstuff marker is a toxic or harmful substance if consumed by a subject. In some embodiments, the foodstuff marker is a bioactive compound that can unintentionally or unexpectedly alter the physiology if consumed by the subject. In some embodiments, the foodstuff marker is indicative of the manner in which the foodstuff was obtained (grown, procured, caught, harvested, processed, cooked, etc.). In some embodiments, the foodstuff marker is indicative of the nutritional content of the foodstuff. In some embodiments, the foodstuff marker is an allergen that can induce an allergic reaction if the foodstuff from which the sample is obtained is consumed by a subject.

In some embodiments, the devices, systems and methods in the present invention further includes receiving or providing a report that indicates the safety or harmfulness for a subject to consume the food stuff from which the sample was obtained based on information including the measured level of the foodstuff marker. The information used to assess the safety of the foodstuff for consumption can include data other than the type and measured amount of the foodstuff marker. These other data can include any health condition associated with the consumer (allergies, pregnancy, chronic or acute diseases, current prescription medications, etc.).

The report can be generated by the device configured to read the CROF device, or can be generated at a remote location upon sending the data including the measured amount of the foodstuff marker. In some cases, a food safety expert can be at the remote location or have access to the data sent to the remote location, and can analyze or review the data to generate the report. The food safety expert can be a scientist or administrator at a governmental agency, such as the US Food and Drug Administration (FDA) or the CDC, a research institution, such as a university, or a private company. In certain embodiments, the food safety expert can send to the user instructions or recommendations based on the data transmitted by the device and/or analyzed at the remote location.

TABLE B9 Foodstuff Markers Source/Class Marker/target Pathogens/ Bacillus anthracis (LF), Giardia lamblia, Legionella, Total Coliforms microbes (including fecal coliform and E. Coli), Viruses (enteric) stapylococci (e.g., Staphylococcus epidermidis and Staphylococcus aureus (enterotoxin A, B, C, G, I, cells, TSST-1), Enterrococcus faecalis, Pseudomonas aeruginosa, Escherichia coli (Shiga-like toxin, F4, F5, H, K, O, bacteriophage K1, K5, K13), other gram-positive bacteria, and gram-negative bacilli. Clostridium difficile (Toxin A, B), Bacteroidetes, Cryptosporidium parvum (GP900, p68 or cryptopain, oocyst), Candida albicans, Bacillus anthracis, Bacillus stearothermophilus, Bacillus cereus, Bacillus licheniformis, Bacillus subtilis, Bacillus pumilus, Bacillus badius, Bacillus globigii, Salmonella typhimurium, Escherichia coli O157:H7, Norovirus, Listeria monocytogenes (internalin), Leptospira interrogans, Leptospira biflexa, Campylobacter jejuni, Campylobacter coli, Clostridium perfringens, Aspergillus flavus (aflatoxins), Aspergillus parasiticus (aflatoxins), Ebola virus (GP), Histoplasma capsulatum, Blastomyces dermatitidis (A antigen), Gram-positive bacteria (teichoic acid), Gram-negative bacteria (such as Pseudomonas aeruginosa, Klebsiella pneumoniae, Salmonella enteriditis, Enterobacter aerogenes, Enterobacter hermanii, Yersinia enterocolitica and Shigella sonnei)(LPS), Polio virus, Influenza type A virus, Disease specific prion (PrP-d), Hepatitis A virus, Toxoplasma gondii, Vibrio cholera, Vibrio parahaemolyticus, Vibrio vulnificus, Enterococcus faecalis, Enterococcus faecium Toxins/ N-methylamino-L-alanine (BMAA), Clostridium botulinum neurotoxins, carcinogens BoNT A, B, Ricin A, B; diphtheria toxin; Aristolochic acid; Colchicine, Ochratoxin A, Sterigmatocystin, Ergotamine, Fumonisins, Fusarin C, domoic acid, Brevetoxin, Mycotoxins Halogenated Heptachlor, chlordane hydrocarbons Heavy metals Lead, mercury, cadmium Allergens peanut (Ara h 1, Ara h 2, Ara h 6), fish, shellfish, mollusks, shrimp (D. pteronyssinus tropomyosin allergen, Der p 10) Cod (Gadc1); Atlantic salmon (Sals1); domestic cattle milk (Bosd4, Bosd5, Bosd6, Bosd7, Bosd8); chicken/egg (Gald1, Gald2, Gald3, Gald4, Gald5); shrimp (Mete1); shrimp (Pena1, Peni1); black tiger shrimp (Penm1, Penm2); squid (Todp1), brown garden snail (Helas1); abalone (Halm1); edible frog (Rane1, Rane2); oriental mustard (Braj1); rapeseed (Bran1); cabbage (Brao3); turnip (Brar1, Brar2); barley (Horv15, Horv16, Horv17, Horv21); rye (Secc20); wheat (Tria18, Tria19, Tria25, Tria26, gliadin); corn (Zeam14, Zeam25); rice (Orys1), celery (Apig1, Apig4, Apig5); carrot (Dauc1, Dauc4); hazelnut (Cora1.04, Cora2, Cora8); strawberry (Fraa1, Fraa3, Fraa4); apple (Mald1, Mald2, Mald3, Mald4); pear (Pyrc1, Pyrc4, Pyrc5); avocado (Persa1); apricot (Pruar1, Pruar3); sweet cherry (Pruav1, Pruav2, Pruav3, Pruav4); European plum (Prud3); almond (Prudu4); peach (Prup3, Prup4); asparagus (Aspao1); saffron crocus (Cros1, Cros2); lettuce (Lacs1); grape (Vitv1); banana (Musxp1); pineapple (Anac1, Anac2); lemon (Citl3); sweet orange (Cits1, Cits2, Cits3); litchi (Litd); yellow mustard (Sinai); soybean (Glym1, Glym2, Glym3, Glym4); mung bean (Vigr1); peanut (Arah1, Arah2, Arah3, Arah4, Arah5, Arah6, Arah7, Arah8); lentil (Lenc1, Lenc2); pea (Piss1, Piss2); kiwi (Actc1, Actc2); bell pepper (Capa1w, Capa2); tomato (Lyce1, Lyce2, Lyce3); potato (Solat1, Solat2, Solat3, Solat4); Brazil nut (Bere1, Bere2); black walnut (Jugn1, Jugn2); English walnut (Jugr1, Jugr2, Jugr3); Cashew (Anao1, Anao2, Anao3); Castor bean (Ricc1); sesame (Sesi1, Sesi2, Sesi3, Sesi4, Sesi5, Sesi6); muskmelon (Cucm1, Cucm2, Cucm3); Chinese-date (Zizm1); Anacardium occidentale (Anao1.0101, Anao1.0102); Apium graveolens (Apig1.0101, Apig1.0201); Daucus carota (Dauc1.0101, Dauc1.0102, Dauc1.0103, Dauc1.0104, Dauc1.0105, Dauc1.0201); Citrus sinensis (Cits3.0101, Cits3.0102); Glycine max (Glym1.0101, Glym1.0102, Glym3.0101, Glym3.0102); Lens culinaris (Lenc1.0101, Lenc1.0102, Lenc1.0103); Pisum sativum (Piss1.0101, Piss1.0102); Lycopersicon esculentum (Lyce2.0101, Lyce2.0102); Fragaria ananassa (Fraa3.0101, Fraa3.0102, Fraa3.0201, Fraa3.0202, Fraa3.0203, Fraa3.0204, Fraa3.0301); Malus domestica (Mald1.0101, Mald1.0102, Mald1.0103, Mald1.0104, Mald1.0105, Mald1.0106, Mald1.0107, Mald1.0108, Mald1.0109, Mald1.0201, Mald1.0202, Mald1.0203, Mald1.0204, Mald1.0205, Mald1.0206, Mald1.0207, Mald1.0208, Mald1.0301, Mald1.0302, Mald1.0303, Mald1.0304, Mald1.0401, Mald1.0402, Mald1.0403, Mald3.0101w, Mald3.0102w, Mald3.0201w, Mald3.0202w, Mald3.0203w, Mald4.0101, Mald4.0102, Mald4.0201, Mald4.0202, Mald4.0301, Mald4.0302); Prunus avium (Pruav1.0101, Pruav1.0201, Pruav1.0202, Pruav1.0203); and Prunus persica (Prup4.0101, Prup4.0201) Synthetic 17beta-estradiol (E2), estrone (EI), estrogen (ES: EI + E2 + estradiol (E3)), hormone 1 7alfa-ethynylestradiol (EE2), 4-nonylphenpol, testosterone, analogues Diethylstilbestrol (DES), recombinant bovine growth hormone (rBGH) Pesticides Dieldrin, carbaryl, chlorpyrifos, parathion, aldrin, endosulfan I, endrin, toxaphene, O-ethyl O-4-nitrophenyl phenylphosphono-thioate (EPN), fenitrothion, pirimiphos-methyl, thiabendazole, methiocarb, Carbendazim, deltamethrin, Avermectin, Carbaryl, Cyanazine, Kresoxim, resmethrin, kadethrin, cyhalothrin, biphenthrin, fenpropathrin, allethrin and tralomethrin; aromatic-substituted alkanecarboxylic acid esters such as fenvarerate, flucythrinate, fluvalinate and cycloprothrin; and non-ester compounds such as etofenprox, halfenprox (MTI-732), 1-(3- phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpentane (MTI-790), 1-(3- phenoxy-4-fluorophenyl)-4-(4-ethoxyphenyl)-4-methylpentane (MTI-800), dimethyl-(4-ethoxyphenyl)-(3-phenoxybenzyloxy)silane (SSI-116), silafluofen and PP-682, carbofuran, triazophos Herbicide atrazine, deethylatrazine, cyanazine, terbuthylazine, terbutryn, molinate, simazine, prometon, promteryn, hydroxyatrazine, 2,6-dichlorobenzamide (BAM), N-dealkylated triazines, mecoprop, thiram, acetochlor, alachlor, Chlorothalonil, Chlorsulfuron, Fenoxaprop ethyl, Linuron, monuron, diuron, Quizalofop-ethyl, Imazalil, Iprodione, Iprovalicarb, Myclobutanil Industrial Dioxin (2,3,7,8-TCDD), 4-tert-octylphenol, bisphenol A (BPA), Styrene, material/waste Di(2-ethylhexyl) phthalate, Dibutyl phthalate (DBP), benzophenone, benzene, trichloroethylene, polychlorinated biphenyl (PCB), nonylphenol, p- cresol, melamine, xylene Antibiotics 3-Amino-5-morpholinomethyl-2-oxazolidone (AMOZ; tissue bound metabolite of furaltadone), oxytetracycline, rolitetracycline, Actinomycin D, Amikacin sulfate, Aminoglycosides, nitrofuran (AOZ), Chloramphenicol, Doxycycline, Streptomycin, gentamicin, neomycin, kanamycin, sulfamethazine, enrofloxacin, sulfadiazine, enrofloxacin Food coloring/ Tartrazine, ethoxyquin, erythritol, penicillin, Fluoroquinolone, Malachite additive/ Green/Leucomalachite Green, C.I. Solvent Yellow 14 (Sudan I), preservative Food Acrylamide, 2-amino-3-methylimidazo(4,5-f)quinolone, Benzo[a]pyrene preparation Nutritional Vitamins A (retinol), B12 (cobalmins), B6 (pyridoxine), B1 (thiamin), B2 content (riboflavin), B3 (niacin), B5 (D-pantothenic acid), B7 (biotin), B9 (folic acid), C, D, E (alpha-tocopherol); Other Caffeine, Ovine myofibril proteins, Etodolac

TABLE B10 POC analytes Disease/Condition Analyte 1. Haematology Complete blood RBCs, WBCs, Platelets count (CBC) 2. Lipid panel Cholesterol level Triglyceride, Total cholesterol, HDL cholesterol, LDL cholesterol 3. Urinalysis Renal Diseases/ pH, Protein, Glucose, Nitrites, Leukocyte esterase, Ketones, Blood cells, Kidney Function Casts, Crystals, Microorganisms, Squamous cells 4. Diabetes Diabetes Glucose, HbA1c, 11-8, CTSS, ITGB2, HLA-DRA, CD53, PLAG27, or MMP9; RBP4; 8-iso-prostaglandin F2α (8-iso-PGF2α), 11-dehydro- thromboxane B2 (TXM), C-peptide, Advanced glycosylation end products (AGEs), 1,5-anhydroglucitol, NGPTL3 and 4, autoantibodies (Zn transporter 8, glutamic acid decarboxylase (GAD)), ATP-binding cassette, sub-family C (CFTR/MRP), member 8; ATP-binding cassette, sub-family C (CFTR/MRP), member 9; angiotensin I converting enzyme (peptidyl- dipeptidase A) 1; adenylate cyclase activating polypeptide 1 (pituitary); adiponectin, C1Q and collagen domain containing; adiponectin receptor 1; adiponectin receptor 2; adrenomedullin; adrenergic, beta-2-, receptor, surface; advanced glycosylation end product-specific receptor; agouti related protein homolog (mouse); angiotensinogen (serpin peptidase inhibitor, clade A, member 8); angiotensin II receptor, type 1; angiotensin II receptor-associated protein; alpha-2-HS-glycoprotein; v-akt murine thymoma viral oncogene homolog 1; v-akt murine thymoma viral oncogene homolog 2; albumin; Alstrom syndrome 1; archidonate 12- lipoxygenase; ankyrin repeat domain 23; apelin, AGTRL 1 Ligand; apolipoprotein A-I; apolipoprotein A-II; apolipoprotein B (including Ag(x) antigen); apolipoprotein E; aryl hydrocarbon receptor nuclear translocator; Aryl hydrocarbon receptor nuclear translocator-like; arrestin, beta 1; arginine vasopressin (neurophysin II, antidiuretic hormone, Diabetes insipidus, neurohypophyseal); bombesin receptor subtype 3; betacellulin; benzodiazepine receptor (peripheral); complement component 3; complement component 4A (Rodgers blood group); complement component 4B (Childo blood group); complement component 5; Calpain- 10; cholecystokinin; cholecystokinin (CCK)-A receptor; chemokine (C-C motif) ligand 2; CD14 molecule; CD163 molecule; CD36 molecule (thrombospondin receptor); CD38 molecule; CD3d molecule, delta (CD3- TCR complex); CD3g molecule, gamma (CD3-TCR complex); CD40 molecule, TNF receptor superfamily member 5; CD40 ligand (TNF superfamily, member 5, hyper-IgM syndrome); CD68 molecule; cyclin- dependent kinase 5; complement factor D (adipsin); CASP8 and FADD- like apoptosis regulator; Clock homolog (mouse); chymase 1, mast cell; cannabinoid receptor 1 (brain); cannabinoid receptor 2 (macrophage); cortistatin; carnitine palmitoyltransferase I; carnitine palmitoyltransferase II; complement component (3b/4b) receptor 1; complement component (3d/Epstein Barr virus) receptor 2; CREB binding protein (Rubinstein- Taybi syndrome); C-reactive protein, pentraxin-related; CREB regulated transcription coactivator 2; colony stimulating factor 1 (macrophage); cathepsin B; cathepsin L; cytochrome P450, family 19, subfamily A, polypeptide 1; Dio-2, death inducer-obliterator 1; dipeptidyl-peptidase 4 (CD26, adenosine deaminase complexing protein 2); epidermal growth factor (beta-urogastrone); early growth response 1; epididymal sperm binding protein 1; ectonucleotide; pyrophosphatase/phosphodiesterase 1; E1A binding protein p300; coagulation factor XIII, A1 polypeptide; coagulation factor VIII, procoagulant component (hemophilia A); fatty acid binding protein 4, adipocyte; Fas (TNF receptor superfamily, member 6); Fas ligand (TNF superfamily, member 6); free fatty acid receptor 1; fibrinogen alpha chain; forkhead box A2; forkhead box O1A; ferritin; glutamate decarboxylase 2; galanin; gastrin; glucagon; glucokinase; gamma-glutamyltransferase 1; growth hormone 1; ghrelin/obestatin preprohormone; gastric inhibitory polypeptide; gastric inhibitory polypeptide receptor; glucagon-like peptide 1 receptor; guanine nucleotide binding protein (G protein), beta polypeptide 3; glutamic-pyruvate transaminase (alanine aminotransferase); gastrin releasing peptide (bombesin); gelsolin (amyloidosis, Finnish type); hemoglobin; hemoglobin, beta; hypocretin (orexin); neuropeptide; precursor; hepatocyte growth factor (hepapoietin A; scatter factor); hepatocyte nuclear factor 4, alpha; haptoglobin; hydroxysteroid (11-beta); dehydrogenase 1; heat shock 70 kDa protein 1B; islet amyloid polypeptide; intercellular adhesion molecule 1 (CD54), human rhinovirus receptor; interferon, gamma; insulin-like growth factor 1 (somatomedin C); insulin-like growth factor 2 (somatomedin A); insulin-like growth factor binding protein 1; insulin-like growth factor binding protein 3; inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta; interleukin 10; interleukin 18 (interferon-gamma-inducing factor); interleukin 1, alpha; interleukin 1, beta; interleukin 1 receptor antagonist; interleukin 2; interleukin 6 (interferon, beta 2); interleukin 6 receptor; interleukin 8; inhibin, beta A (activin A, activin AB alpha polypeptide); insulin; insulin receptor; insulin promoter factor-1; insulin receptor substrate 1; insulin receptor substrate-2; potassium inwardly-rectifying channel, subfamily J, member 11; potassium inwardly-rectifying channel, subfamily J, member 8; klotho; kallikrein B, plasma (Fletcher factor) 1; leptin (obesity homolog, mouse); leptin receptor; legumain; lipoprotein, Lp(a); lipoprotein lipase; v- maf musculoaponeurotic brosarcoma oncogene homolog A (avian); mitogen-activated protein kinase 8; interacting protein 1; mannose-binding lectin (protein C) 2, soluble (opsonic defect); melanocortin 4 receptor; melanin-concentrating hormone receptor 1; matrix metallopeptidase 12 (macrophage elastase); matrix metallopeptidase 14 (membrane-inserted); matrix metallopeptidase 2 (gelatinase A, 72 kDa gelatinase, 72 kDa type IV collagenase); matrix metallopeptidase 9 (gelatinase B, 92 kDa gelatinase, 92 kDa type IV collagenase); nuclear receptor co-repressor 1; neurogenic differentiation 1; nuclear factor of kappa light polypeptide gene enhancer in B-cells 1(p105); nerve growth factor, beta polypeptide; non- insulin-dependent Diabetes Mellitus (common, type 2) 1; non-insulin- dependent Diabetes Mellitus (common, type 2) 2; Noninsulin-dependent Diabetes Mellitus 3; nischarin (imidazoline receptor); NF-kappaB repressing factor; neuronatin; nitric oxide synthase 2A; Niemann-Pick disease, type C2; natriuretic peptide precursor B; nuclear receptor subfamily 1, group D, member 1; nuclear respiratory factor 1; oxytocin, prepro-(neurophysin I); purinergic receptor P2Y, G-protein coupled, 10; purinergic receptor P2Y, G-protein coupled, 12; purinergic receptor P2Y, G-protein coupled, 2; progestagen-associated endometrial; protein (placental protein 14, pregnancy-associated endometrial alpha-2-globulin, alpha uterine protein); paired box gene 4; pre-B-cell colony enhancing factor 1; phosphoenolpyruvate carboxykinase 1 (PEPCK1); proprotein convertase; subtilisin/kexin type 1; placental growth factor, vascular; endothelial growth factor-related protein; phosphoinositide-3-kinase, catalytic, alpha polypeptide; phosphoinositide-3-kinase, regulatory subunit 1 (p85 alpha); phospholipase A2, group XIIA; phospholipase A2, group IID; plasminogen activator, tissue; patatin-like phospholipase domain containing 2; proopiomelanocortin (adrenocorticotropin/beta- lipotropin/alpha-melanocyte stimulating hormone/beta- melanocyte stimulating hormone/beta-endorphin); paraoxonase 1 ESA, PON, Paraoxonase; peroxisome proliferative activated receptor, alpha; peroxisome proliferative activated receptor, delta; peroxisome proliferative activated receptor, gamma; peroxisome proliferative activated receptor, gamma, coactivator 1; protein phosphatase 1, regulatory (inhibitor) subunit 3A (glycogen and sarcoplasmic reticulum binding subunit, skeletal muscle); protein phosphatase 2A, regulatory subunit B′(PR 53); protein kinase, AMP-activated, beta 1 non-catalytic subunit; protein kinase, cAMP-dependent, catalytic, alpha; protein kinase C, epsilon; proteasome (prosome, macropain) 26S subunit, non-ATPase, 9 (Bridge-1); prostaglandin E synthase; prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase); protein tyrosine phosphatase, mitochondrial 1; Peptide YY retinol binding protein 4, plasma (RBP4); regenerating islet-derived 1 alpha (pancreatic stone protein, pancreatic thread protein); resistin; ribosomal protein S6 kinase, 90 kDa, polypeptide 1; Ras-related associated with Diabetes; serum amyloid A1; selectin E (endothelial adhesion molecule 1); serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6; serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1; serum/glucocorticoid regulated kinase; sex hormone-binding globulin; thioredoxin interacting protein; solute carrier family 2, member 10; solute carrier family 2, member 2; solute carrier family 2, member 4; solute carrier family 7 (cationic amino acid transporter, y+ system), member 1(ERR); SNF1-like kinase 2; suppressor of cytokine signaling 3; v-src sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog (avian); sterol regulatory element binding transcription factor 1; solute carrier family 2, member 4; somatostatin receptor 2; somatostatin receptor 5; transcription factor 1, hepatic; LF-B1, hepatic nuclear factor (HNF1); transcription factor 2, hepatic, LF-B3, variant hepatic nuclear factor; transcription factor 7-like 2 (T-cell specific, HMG- box); transforming growth factor, beta 1 (Camurati-Engelmann disease); transglutaminase 2 (C polypeptide, protein-glutamine-gamma- glutamyltransferase); thrombospondin 1; thrombospondin, type I, domain containing 1; tumor necrosis factor (TNF superfamily, member 2); tumor necrosis factor (TNF superfamily, member 2); tumor necrosis factor receptor superfamily, member 1A; tumor necrosis factor receptor superfamily, member 1B; tryptophan hydroxylase 2; thyrotropin-releasing hormone; transient receptor potential cation channe1, subfamily V, member 1; thioredoxin interacting protein; thioredoxin reductase 2; urocortin 3 (stresscopin); uncoupling protein 2 (mitochondria1, proton carrier); upstream transcription factor 1; urotensin 2; vascular cell adhesion molecule 1; vascular endothelial growth factor; vimentin; vasoactive intestinal peptide; vasoactive intestinal peptide receptor 1; vasoactive intestinal peptide receptor 2; von Willebrand factor; Wolfram syndrome 1 (wolframin); X-ray repair complementing defective repair in Chinese hamster cells 6; c-peptide; cortisol; vitamin D3; estrogen; estradiol; digitalis-like factor; oxyntomodulin; dehydroepiandrosterone sulfate (DHEAS); serotonin (5-hydroxytryptamine); anti-CD38 autoantibodies; gad65 autoantibody; Angiogenin, ribonuclease, RNase A family, 5; Hemoglobin A1c; Intercellular adhesion molecule 3 (CD50); interleukin 6 signal transducer (gp130, oncostatin M receptor); selectin P (granule embrane protein 140 kDa, antigen CD62); TIMP metallopeptidase inhibitor; Proinsulin; endoglin; interleukin 2 receptor, beta; insulin-like growth factor binding protein 2; insulin-like growth factor 1 receptor; fructosamine, N-acetyl-beta-d- glucosaminidase, pentosidine, advanced glycation end product, beta2- microglobulin, pyrraline 5. Sexually Transmitted Diseases Chlamydia bacteria Chlamydia trachomatis Gonorrhea bacteria Neisseria gonorrhoeae Syphilis Antibodies, bacterial DNA Trichomonas protzoan Trichomoniasis Human DNA or RNA of HPV virus papillomavirus (HPV) Genital herpes Antibodies Human HIV antigen p24, Antibodies Immunodeficiency Virus (HIV) 6. Other Infectious Diseases Ebola Antigen, IgM and IgG antibodies, RNA Malaria Antigen, Nucleic acids, Antibodies Hepatitis B and Viral proteins, Antibodies, Viral DNA Hepatitis C Influenza Viral proteins, Antibodies, Viral DNA 7. Cardiac testing Cardiac markers Troponin (I or T), Creatine Kinase (CK) and CK-MB, Myoglobin, hs-CRP, BNP and NT-proBNP 8. Female Reproduction testing Pregnancy test HCG (human chorionic gonadotropin) Ovulation test LH (luteinizing hormone) 9. Drugs of Abuse Alcohol Ethanol, ethyl glucuronide Cocaine Cocaine, Benzolecgonine, Ecgonine, Ecgonine Methyl Ester Heroine Heroine, 6MAM, Morphine PCP PCP, Phencyclidine Thienylcyclohexylpiperidine (TCP) Amphetamines Amphetamines (such as D-Amphetamine, D-Methamphetamine, L- Amphetamine, L-Methamphetamine, 3,4-Methylenedioxy- methamphetamine (MDMA), 3,4-Methylenedioxyamphetamine (MDA), 3,4-Methylenedioxyethylamphetamine (MDEA), Paramethoxyamphetamine (PMA)) Methamphetamine D-Methamphetamine, D-Amphetamine, L-Methamphetamine, Chloroquine, (+/−) Ephedrine, 3,4-Methylenedioxy-methamphetamine (MDMA), 3,4-Methylenedioxyamphetamine (MDA), 3,4- Methylenedioxyethylamphetamine (MDEA), Procaine MDMA (Ecstasy) MDMA, MDA, MDEA, D-Amphetamine, D-Methamphetamine, Paramethoxyamphetamine (PMA) Barbiturates Secobarbital, Phenobarbital, Butalbital, Allobarbital, Alphenal, Amorbarbital, Aprobarbital, Hexobarbital, Butabarbital, Pentobarbital Phenobarbital Phenobarbital, Butalbital, Amobarbital, Secobarbital Benzodiazepines Oxazepam, Alprazolam, Bromazepam, Chlordiazepoxide, Clobazam, Clonazepam, Clorazepate, Delorazepam, Desalkyflurazepam, Diazepam, Estazolam, Fentanyl, Flunitrazepam (Rohypnol ®), Flurazepam, a- Hydroxyalprazolam, Lorazepam (Ativan ®), Lormetazepam, Medazepam, Midazolam, Nitrazepam, Nordiazepam, Prazepam, Temazepam, Tetrazepam Cannabis Δ9-THC, 11-Nor-Δ8-THC-9-COOH, 11-Nor-Δ9-THC-9-COOH, 11- (Marijuana, etc.) Hydroxy-Δ9-tetrahydrocannabinol, Δ8-Tetrahydrocannabinol, Δ9- Tetrahydrocannabinol, Cannabinol, Cannabidiol, pentanoic acid, butanoic acid, 4-hydroxybutyl, 4-hydroxypentyl Codeine Morphine, Codeine, Diacetyl morphine (heroine), Ethylmorphine, Hydromorphone, Meperidine, 6-Monoacetylmorphine, Morphine-3- glucuronide, Oxycodone, Oxymorphone, Promethazine, Rifampicine, Thebaine, Trimipamine Nicotine/Cotinine Cotinine, Nicotine Morphine Morphine Tricyclic Nortriptyline, Amitriptyline, Chlorpromazine, Clomipramine, antidepressants Cyclobenzaprine, Desipramine, Diphenyldramine, Doxepine, Imipramine, (TCA's) Nordoxepine, Opipramol, Protriptyline, Perphenazine, Promazine, Promethazine, Trimipramine LSD LSD Methadone EDDP, Doxylamine, Methadone, Methadol Methaqualone Methaqualone, 3-hydroxy methaqualone, 4-hydroxy methaqualone, 2- hydroxy methaqualone, Amitriptyline, Carbamazepine, Nortriptyline, Phenytoin, Primidone, Theophyline buprenorphine Buprenorphine, Buprenorphine-3-B-d-gluconoride, Nor-Buprenorphine, Nor-Buprenorphine-3-B-d-gluconoride Ketamine Ketamine, Norketamine, Dextromethorphan, Dextrorphantartrate, EDDP, Phencyclidine, Promazine, Meperidine, D-Methamphetamine, Mephentermine h.s., MDEA, Nordoxepin hydrochloride, Promethazine, D- Norpropoxyphene, Methadone MethCathinone MethCathinone, 4-MMC (Mephedrone), 3-MMC (3-methylmethcathinone), 4-MEC (4-methylethcathinone), Methylone (MDMC, bk-MDMA), Cathinone, MDPV MDPV MDPV, Cathinone, MethCathinone methylphenidate methylphenidate tramadol Tramadol, N-demethyl-tramadol, O-demethyl-tramadol oxycodone Oxycodone, Oxymorphone, Codeine, Diacetyl Morphine (Heroine), Ethylmorphine, Hydrocodone, Hydromorphone, Merperidine, 6- Monoacetylmorphine, Morphine, Morphine-3-beta-D-glucuronide, Thebaine propoxyphene D-propoxyphene, D-norpropoxyphene Fentanyl Methaqualone, Mecloqualone, 3-hydroxy methaqualone, 4-hydroxy methaqualone, 2-hydroxy methaqualone, Amitriptyline, Carbamazepine, Nortriptyline, Phenytoin, Primidone, Theophyline 10. Coagulation Disorders Congenital Platelet, Fibronogen, Factor V, Anti-Xa, Factor XIII screen, D-dimer hemophilia; Von Willebrand disease; Acquired hemophilia 11. Fecal Occult Blood Test Colon Cancer; Blood cells, Hemoglobin, Fecal DNA colon polyps; crohn's disease; hemorrhoids; anal fissures; intestinal infections; Ulcers; Ulcerative colitis 12. Blood Gas and Electrolytes pH, pCO₂, pO₂, Sodium (Na+), Potassium (K+), Calcium (Ca++), HCO3, TCO2, SBE

The health conditions that can be diagnosed or measured by the subject method, device and system include, but are not limited to: chemical balance; nutritional health; exercise; fatigue; sleep; stress; prediabetes; allergies; aging; exposure to environmental toxins, pesticides, herbicides, synthetic hormone analogs; pregnancy; menopause; and andropause.

In certain embodiments, relative levels of nucleic acids in two or more different nucleic acid samples can be obtained using the above methods, and compared. In these embodiments, the results obtained from the above-described methods are usually normalized to the total amount of nucleic acids in the sample (e.g., constitutive RNAs), and compared. This can be done by comparing ratios, or by any other means. In particular embodiments, the nucleic acid profiles of two or more different samples can be compared to identify nucleic acids that are associated with a particular disease or condition.

In some examples, the different samples can consist of an “experimental” sample, i.e., a sample of interest, and a “control” sample to which the experimental sample can be compared. In many embodiments, the different samples are pairs of cell types or fractions thereof, one cell type being a cell type of interest, e.g., an abnormal cell, and the other a control, e.g., normal, cell. If two fractions of cells are compared, the fractions are usually the same fraction from each of the two cells. In certain embodiments, however, two fractions of the same cell can be compared. Exemplary cell type pairs include, for example, cells isolated from a tissue biopsy (e.g., from a tissue having a disease such as colon, breast, prostate, lung, skin cancer, or infected with a pathogen etc.) and normal cells from the same tissue, usually from the same patient; cells grown in tissue culture that are immortal (e.g., cells with a proliferative mutation or an immortalizing transgene), infected with a pathogen, or treated (e.g., with environmental or chemical agents such as peptides, hormones, altered temperature, growth condition, physical stress, cellular transformation, etc.), and a normal cell (e.g., a cell that is otherwise identical to the experimental cell except that it is not immortal, infected, or treated, etc.); a cell isolated from a mammal with a cancer, a disease, a geriatric mammal, or a mammal exposed to a condition, and a cell from a mammal of the same species, preferably from the same family, that is healthy or young; and differentiated cells and non-differentiated cells from the same mammal (e.g., one cell being the progenitor of the other in a mammal, for example). In one embodiment, cells of different types, e.g., neuronal and non-neuronal cells, or cells of different status (e.g., before and after a stimulus on the cells) can be employed. In another embodiment of the invention, the experimental material is cells susceptible to infection by a pathogen such as a virus, e.g., human immunodeficiency virus (HIV), etc., and the control material is cells resistant to infection by the pathogen. In another embodiment of the invention, the sample pair is represented by undifferentiated cells, e.g., stem cells, and differentiated cells.

7. Control and Measure the Sample Thickness without Using Spacers

In some embodiments of the present invention, the spacers that are used to regulate the sample or a relevant volume of the sample are replaced by (a) positioning sensors that can measure the plate inner spacing, and (b) the devices that can control the plate positions and move the plates into a desired plate inner spacing based on the information provided the sensors. In some embodiment, all the spacers are replaced by translation stage, monitoring sensors and feedback system.

Measuring of Spacing and/or Sample Thickness Using Optical Method.

In some embodiments, the measuring (f) of the spacing between the inner surfaces comprises the use of optical interference. The optical interference can use multiple wavelength. For example, the light signal due to the interference of a light reflected at the inner surface of the first plate and the second plate oscillate with the wavelength of the light. From the oscillation, one can determine the spacing between the inner surfaces. To enhance the interference signal, one of the inner surfaces or both can be coated with light reflection material.

In some embodiments, the measuring (f) of the spacing between the inner surfaces comprises taking optical imaging (e.g. taking a 2D (two-dimensional)/3D (three-dimensional) image of the sample and the image taking can be multiple times with different viewing angles, different wavelength, different phase, and/or different polarization) and image processing.

Measuring of Entire Sample Area or Volume Using Optical Methods.

In some embodiments, the measuring (f) of the entire sample area or volume comprises taking optical imaging (e.g. taking a 2D (two-dimensional)/3D (three-dimensional) image of the sample and the image taking can be multiple times with different viewing angles, different wavelength, different phase, and/or different polarization) and image processing. The sample area means the area in the direction approximately parallel to the first plate and the second plate. The 3D imaging can use the method of fringe projection profilometry (FPP), which is one of the most prevalent methods for acquiring three-dimensional (3D) images of objects.

In some embodiments, the measuring of the sample area or volume by imaging comprises (a) calibration of the image scale by using a sample of the known area or volume (e.g., The imager is a smartphone and the dimensions of the image taken by the phone can be calibrated by comparing an image of the a sample of known dimension taken the same phone); (b) comparison of the image with the scale markers (rulers) placed on or near the first plate and second plate (discussed further herein), and (c) a combination of thereof.

As used herein, light can include visible light, ultraviolet light, infrared light, and/or near infrared light. Light can include wavelengths in the range from 20 nm to 20,000 nm.

It must be noted that as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise, e.g., when the word “single” is used. For example, reference to “an analyte” includes a single analyte and multiple analytes, reference to “a capture agent” includes a single capture agent and multiple capture agents, reference to “a detection agent” includes a single detection agent and multiple detection agents, reference to “an agent” includes a single agent and multiple agents, and reference to “a camera” includes a single camera and multiple cameras.

As used herein, the terms “adapted” and “configured” mean that the element, component, or other subject matter is designed and/or intended to perform a given function. Thus, the use of the terms “adapted” and “configured” should not be construed to mean that a given element, component, or other subject matter is simply “capable of” performing a given function. Similarly, subject matter that is recited as being configured to perform a particular function can additionally or alternatively be described as being operative to perform that function.

As used herein, the phrase, “for example,” the phrase, “as an example,” and/or simply the terms “example” and “exemplary” when used with reference to one or more components, features, details, structures, embodiments, and/or methods according to the present disclosure, are intended to convey that the described component, feature, detail, structure, embodiment, and/or method is an illustrative, non-exclusive example of components, features, details, structures, embodiments, and/or methods according to the present disclosure. Thus, the described component, feature, detail, structure, embodiment, and/or method is not intended to be limiting, required, or exclusive/exhaustive; and other components, features, details, structures, embodiments, and/or methods, including structurally and/or functionally similar and/or equivalent components, features, details, structures, embodiments, and/or methods, are also within the scope of the present disclosure.

As used herein, the phrases “at least one of” and “one or more of,” in reference to a list of more than one entity, means any one or more of the entity in the list of entity, and is not limited to at least one of each and every entity specifically listed within the list of entity. For example, “at least one of A and B” (or, equivalently, “at least one of A or B,” or, equivalently, “at least one of A and/or B”) may refer to A alone, B alone, or the combination of A and B.

As used herein, the term “and/or” placed between a first entity and a second entity means one of (1) the first entity, (2) the second entity, and (3) the first entity and the second entity. Multiple entity listed with “and/or” should be construed in the same manner, i.e., “one or more” of the entity so conjoined. Other entity may optionally be present other than the entity specifically identified by the “and/or” clause, whether related or unrelated to those entity specifically identified. Thus, as a non-limiting example, a reference to “A and/or B,” when used in conjunction with open-ended language such as “comprising” may refer, in some embodiments, to A only (optionally including entity other than B); in certain embodiments, to B only (optionally including entity other than A); in yet certain embodiments, to both A and B (optionally including other entity). These entity may refer to elements, actions, structures, steps, operations, values, and the like.

In the event that any patents, patent applications, or other references are incorporated by reference herein and (1) define a term in a manner that is inconsistent with and/or (2) are otherwise inconsistent with, either the non-incorporated portion of the present disclosure or any of the other incorporated references, the non-incorporated portion of the present disclosure shall control, and the term or incorporated disclosure therein shall only control with respect to the reference in which the term is defined and/or the incorporated disclosure was present originally.

It is believed that the following claims particularly point out certain combinations and subcombinations that are directed to one of the disclosed inventions and are novel and non-obvious. Inventions embodied in other combinations and subcombinations of features, functions, elements and/or properties may be claimed through amendment of the present claims or presentation of new claims in this or a related application. Such amended or new claims, whether they are directed to a different invention or directed to the same invention, whether different, broader, narrower, or equal in scope to the original claims, are also regarded as included within the subject matter of the inventions of the present disclosure. 

The invention claimed is:
 1. A method of forming a thin sample layer with a uniform predetermined thickness by pressing with an imprecise pressing force, comprising: (a) providing a device comprising a first plate, a second plate, and spacers, wherein: i. the plates are movable relative to each other into different configurations; ii. at least one of the first plate or the second plate is flexible; iii. each of the plates comprises an inner surface that has a sample contact area for contacting a sample containing or suspected of containing an analyte; iv. each of the plates comprises, on its respective outer surface, a force area for applying an imprecise pressing force that forces the plates together; v. one or both of the plates comprise the spacers that are permanently fixed on the inner surface of a respective plate, vi. the spacers have a predetermined substantially uniform height that is equal to or less than 200 microns, and a predetermined fixed inter-spacer-distance between adjacent spacers; vii. the fourth power of the inter-spacer-distance (ISD) divided by the thickness (h) and the Young's modulus (E) of the at least one flexible plate (ISD⁴/(hE)) is 5×10⁵ um²/GPa or less; viii. the thickness of the at least one flexible plate times the Young's modulus of the at least one flexible plate is in the range 60 to 750 GPa-um; and ix. at least one of the spacers is inside the sample contact area; (b) depositing the sample on one or both of the plates; when the plates are configured in an open configuration, wherein the open configuration is a configuration in which the two plates are partially or completely separated apart and the spacing between the plates is not regulated by the spacers; (c) after (b), applying an imprecise pressing force on the force areas to bring the two plates into a closed configuration, in which: at least a part of the sample is compressed by the two plates into a layer of substantially uniform thickness; wherein the layer of substantially uniform thickness is confined by the sample contact surfaces of the plates and is regulated by the plates and the spacers; wherein the imprecise pressing force has a magnitude that is not precisely known or precisely predictable at the time the imprecise pressing force is applied.
 2. The method of claim 1, further comprising a step of using an area-determination device to determine a lateral area of a relevant volume of the sample in a closed configuration of the plate.
 3. The method of claim 2, wherein the area-determination device comprises a camera.
 4. The method of claim 1, wherein the imprecise pressing force has a magnitude in a range of 1N to 20 N and/or a pressure in a range of 0.1 psi to 280 psi.
 5. The method of claim 2, wherein the area-determination device comprises a camera and an area in the sample contact area of a plate, and wherein the area is in contact with the sample.
 6. The method of claim 1, wherein the imprecise pressing force is in a range of 20 N to 200 N.
 7. The method of claim 1, wherein the device is further configured to have, after the imprecise pressing force is removed, a sample thickness that is substantially the same in thickness and uniformity as that when the imprecise pressing force is applied.
 8. The method of claim 1, wherein the imprecise pressing force is provided by human hand.
 9. The method of claim 1, wherein the imprecise pressing force has a pressure in a range of 0.01 kg/cm² (centimeter square) to 100 kg/cm².
 10. The method of claim 1, wherein the spacers are in a periodic array form in the area of the uniform sample thickness area.
 11. The method of claim 1, wherein a multiplication product of a filling factor and the Young's modulus of the spacers is 2 MPa or larger.
 12. The method of claim 1, wherein the imprecise pressing force is applied by human hand directly or indirectly.
 13. The method of claim 1, wherein the imprecise pressing force applied is in a range of 1 N to 20 N.
 14. The method of claim 1, wherein the layer of substantially uniform thickness has a thickness that varies by less than 15%, 10%, or 5% of an average thickness.
 15. The method of claim 1, wherein the imprecise pressing force is applied by pinching the device between a thumb and forefinger.
 16. The method of claim 1, wherein the imprecise pressing force has a variation that is at least 20% of the total force that is applied.
 17. The method of claim 1, wherein the device holds itself in the closed configuration after the imprecise pressing force used in the pressing has been removed.
 18. The method of claim 1, wherein the uniform thickness sample layer area is larger than that area upon which the imprecise pressing force is applied.
 19. The method of claim 1, wherein the imprecise pressing force has a pressure in a range of 0.1 kg/cm² to 10 kg/cm².
 20. The method of claim 1, wherein the imprecise pressing force is not predetermined beforehand and is not measured.
 21. The method of claim 1, wherein the analyte comprises a molecule, cells, tissues, viruses, and nanoparticles with different shapes, wherein the molecule comprises a protein, peptides, DNA, RNA, nucleic acid, or other molecule.
 22. The method of claim 1, wherein the analyte comprises white blood cells, red blood cells and platelets.
 23. The method of claim 1, wherein the analyte is stained.
 24. The method of claim 1, wherein the inter-spacer-distance (ISD) is equal or less than about 120 um (micrometer).
 25. The method of claim 1, wherein the inter-spacer-distance (ISD) is equal or less than about 100 urn (micrometer).
 26. The method of claim 1, wherein a multiplication product of a filling factor and the Young's modulus of the spacers is between 20 to 150 MPa.
 27. The method of claim 1, wherein the fourth power of the inter-spacer-distance (ISD) divided by the thickness (h) and the Young's modulus (E) of the at least one flexible plate (ISD⁴/(hE)) is 5×10⁵ um³/GPa or less.
 28. The method of claim 1, wherein the spacers have pillar shape, a substantially flat top surface, a predetermined substantially uniform height, and a predetermined constant inter-spacer-distance between adjacent spacers that is at least about 2 times larger than the size of the analyte, wherein the Young's modulus of the spacers times the filling factor of the spacers is equal or larger than 2 MPa, wherein the filling factor is the ratio of the spacer contact area to the total plate area, and wherein, for each spacer, the ratio of the lateral dimension of the spacer to its height is at least
 1. 29. The method of claim 1, wherein the spacers have pillar shape, a flat top surface, a predetermined substantially uniform height and a predetermined constant inter-spacer-distance between adjacent spacers, wherein the Youngs modulus of the spacers times the filling factor of the spacers is equal or larger than 20 MPa, wherein the filling factor is the ratio of the spacer contact area to the total plate area, and wherein, for each spacer, the ratio of the lateral dimension of the spacer to its height is at least 1 (one), wherein the fourth power of the inter-spacer-distance (ISD) divided by the thickness (h) and the Young's modulus (E) nt the at least one flexible plate (ISD⁴/(hE)) is 5×10⁵ um³/GPa or less, and wherein a thickness of the at least one flexible plate times the Young's modulus of the at least one flexible plate is in the range of 100 to 550 GPa-um.
 30. The method of claim 1, wherein the device further comprises a dry reagent coated on one or both plates.
 31. The method of claim 1, wherein a thickness of the at least one flexible plate times the Young's modulus of the at least one flexible plate is in the range of 100 to 550 GPa-um.
 32. The method of claim 1, wherein the sample is a biological sample selected from amniotic fluid, aqueous humour, vitreous humour, blood, breast milk, cerebrospinal fluid (CSF), cerumen (earwax), chyle, chime, endolymph, perilymph, feces, breath, gastric acid, gastric juice, lymph, mucus, pericardial fluid, peritoneal fluid, pleural fluid, pus, rheum, saliva, exhaled breath condensates, sebum, semen, sputum, sweat, synovial fluid, tears, vomit, and urine.
 33. The method of claim 1, wherein the spacers have a shape of pillars and a ratio of the width to the height of the pillar is equal or larger than
 2. 34. The method of claim 1, wherein the sample that is deposited on one or both of the plates has an unknown volume.
 35. The method of claim 1, wherein the sample is for a detection, purification and quantification of chemical compounds or biomolecules that correlates with a stage of certain diseases.
 36. The method of claim 1, wherein the sample is related to infectious and parasitic disease, injuries, cardiovascular disease, cancer, mental disorders, neuropsychiatric disorders, pulmonary diseases, renal diseases, and other and organic diseases.
 37. The method of claim 1, wherein the sample is related to a detection, purification and quantification of a microorganism.
 38. The method of claim 1, wherein the sample is related to virus, fungus and bacteria from the environment.
 39. The method of claim 1, wherein the sample is related to a detection, quantification of chemical compounds or biological samples that pose a hazard to food safety or national security.
 40. The method of claim 1, wherein the sample is related to quantification of vital parameters in medical or physiological monitor.
 41. The method of claim 1, wherein the sample is related to glucose, blood, oxygen level, total blood count.
 42. The method of claim 1, wherein the sample is related to the detection and quantification of specific DNA or RNA from biosamples.
 43. The method of claim 1, wherein one or both plates comprise a location marker, a scaling marker, or an image marker.
 44. The method of claim 1, wherein the sample is related to a detection of reaction products, e.g., during synthesis or purification of pharmaceuticals.
 45. The method of claim 1, wherein the sample is the sample in a detection of proteins, peptides, nucleic acids, synthetic compounds, or inorganic compounds.
 46. The method of claim 1, wherein the sample is the sample in the fields of human, veterinary, agriculture, foods, environments, and drug testing.
 47. The method of claim 1, wherein the sample is a biological sample is selected from blood, serum, plasma, a nasal swab, a nasopharyngeal wash, saliva, urine, gastric fluid, spinal fluid, tears, stool, mucus, sweat, earwax, oil, a glandular secretion, cerebral spinal fluid, tissue, semen, vaginal fluid, interstitial fluids derived from tumorous tissue, ocular fluids, spinal fluid, a throat swab, breath, hair, finger nails, skin, biopsy, placental fluid, amniotic fluid, cord blood, lymphatic fluids, cavity fluids, sputum, pus, microbiota, meconium, breast milk, exhaled condensate nasopharyngeal wash, throat swab, stool samples, hair, finger nail, ear wax, breath, connective tissue, muscle tissue, nervous tissue, epithelial tissue, cartilage, cancerous sample, or bone.
 48. The method of claim 1, wherein the device further comprises, on one or both plates, one or a plurality of dry binding sites and/or one or a plurality of reagent sites.
 49. The method of claim 1, wherein the spacers function as a location marker, a scale marker, an imaging marker, or any combination thereof.
 50. The method of claim 1, wherein the layer of substantially uniform thickness has a value in the range of 0.5 um to 30 um.
 51. The method of claim 1, wherein the imprecise pressing force is applied by conformal pressing.
 52. The method of claim 1, wherein the materials of the plate and the spacers are selected from polystyrene, PMMA, PC, COC, COP, or another plastic. 